SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4366224 | snp | A/G | 0.490622 | 0.0678316 | intron-variant | ASB11 | GRCh38.p7 | X:15306079 | CCTCCAGCTCCATCC[A/G]TGTCTCTGCAAAGGA | 140456 |
rs4370686 | snp | C/T | 0.491815 | 0.0634477 | intron-variant | ASB11 | GRCh38.p7 | X:15306032 | ATGTGGCATTTGGTT[C/T]TCTGTTCCTGTTAGT | 140456 |
rs4830529 | snp | A/T | 0.00633741 | 0.0559334 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315720 | CTCCTGTTACCGAGA[A/T]CTCTGTAGGTTCTAA | 140456 |
rs4830935 | snp | A/C | 0.327237 | 0.23777 | | | GRCh38.p7 | X:15278266 | ATAATGTCATAAAAA[A/C]CAGATGATTAGTCTG | 140456 |
rs5008833 | snp | C/T | 0.481456 | 0.0944889 | intron-variant | ASB11 | GRCh38.p7 | X:15294611 | CCTGGGTTCAAATGA[C/T]CCTCCTGCCTCAGCC | 140456 |
rs5901555 | in-del | -/TC | 0.488319 | 0.0755258 | intron-variant | ASB11 | GRCh38.p7 | X:15294882 | GATTTCCTATAAATT[-/TC]TCTCTTAGTTCACGT | 140456 |
rs5901557 | in-del | -/TCTTA | | | intron-variant | ASB11 | GRCh38.p7 | X:15305777 | GTTTTTTGACTTTTA[-/TCTTA]AGTTCAGGGGTACAT | 140456 |
rs5934230 | snp | G/T | 0.499997 | 0.00128534 | intron-variant | ASB11 | GRCh38.p7 | X:15289981 | GTGAGCCGAGATAGC[G/T]CCACTGCACTCCAGC | 140456 |
rs5934231 | snp | C/T | 0.474111 | 0.11079 | intron-variant | ASB11 | GRCh38.p7 | X:15291764 | TTATATGGCTGAGCA[C/T]GGTGGCTCATGCCTG | 140456 |
rs5934232 | snp | A/T | 0.454162 | 0.144284 | intron-variant | ASB11 | GRCh38.p7 | X:15295243 | AGACGGGGTTTCACC[A/T]TGTTGGCCAGGATGG | 140456 |
rs5934233 | snp | C/G | 0.415877 | 0.188383 | intron-variant | ASB11 | GRCh38.p7 | X:15299108 | ACCATTTCCCTCCCT[C/G]TGATGATCACGTTCT | 140456 |
rs5935921 | snp | C/T | 0.488319 | 0.0755258 | | | GRCh38.p7 | X:15275854 | TCCTGGTACAGGCTC[C/T]GCTAAGGGAAGGAGA | 140456 |
rs5935922 | snp | A/G | 0.493114 | 0.0582701 | | | GRCh38.p7 | X:15278997 | TTCAATATTTGGGGC[A/G]CATTGAATTGTACCT | 140456 |
rs5935923 | snp | G/T | 0.476119 | 0.10663 | | | GRCh38.p7 | X:15279538 | TGCCTTTGATATATT[G/T]CAAAAATGCTTTCCC | 140456 |
rs5935924 | snp | C/G | 0.492736 | 0.0598256 | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281434 | ACAAAAGTGAAACTC[C/G]GTCTAAAAAAGAAAA | 140456 |
rs5935925 | snp | A/G | 0.491541 | 0.0644807 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283411 | CATTTAAAGATACTA[A/G]GAGTCTAAGCTGTTG | 140456 |
rs5935926 | snp | A/G | 0.491679 | 0.0639643 | intron-variant | ASB11 | GRCh38.p7 | X:15287159 | TCACCATTTAGTCGG[A/G]TTTCTGAAATACTCT | 140456 |
rs5935927 | snp | C/T | 0.481456 | 0.0944889 | intron-variant | ASB11 | GRCh38.p7 | X:15287403 | GTGATCTCTGCTCAT[C/T]GCAACCTCCGCCTCC | 140456 |
rs5935928 | snp | G/T | 0.482063 | 0.0929878 | intron-variant | ASB11 | GRCh38.p7 | X:15289062 | TAGATTTCCCAAAGG[G/T]AAACCACCCTCTTGT | 140456 |
rs5935929 | snp | A/G | 0.474111 | 0.11079 | intron-variant | ASB11 | GRCh38.p7 | X:15289369 | ACTCATTTCTCTAGA[A/G]AAGTTTTGTTTTTAG | 140456 |
rs5935930 | snp | C/T | 0.453679 | 0.144965 | intron-variant | ASB11 | GRCh38.p7 | X:15289441 | ACAAGAACTTCATCT[C/T]TGAAGCTGTAGAAAA | 140456 |
rs5935931 | snp | A/T | 0.474231 | 0.110546 | intron-variant | ASB11 | GRCh38.p7 | X:15292627 | CAGCCTTTTCTTTTC[A/T]ATAACTATGACCTTG | 140456 |
rs5935932 | snp | A/G | 0.454001 | 0.144511 | intron-variant | ASB11 | GRCh38.p7 | X:15292966 | AAGCATTCCGAAGTT[A/G]TAAGTAGGGCTCTTT | 140456 |
rs5935933 | snp | A/G | 0.45384 | 0.144738 | intron-variant | ASB11 | GRCh38.p7 | X:15294387 | GTTGCAATATAACCC[A/G]TGAAACAGGGTCTTG | 140456 |
rs5935934 | snp | C/T | 0.415597 | 0.187291 | intron-variant | ASB11 | GRCh38.p7 | X:15295283 | CTTGATCTCATGATC[C/T]ACCTGCCTCAGCCTC | 140456 |
rs5935935 | snp | C/T | 0.398695 | 0.200972 | intron-variant | ASB11 | GRCh38.p7 | X:15296257 | GACTCTGTCTAAAAA[C/T]AAAAAGATGGAAAAA | 140456 |
rs5935936 | snp | C/T | 0.474948 | 0.109081 | intron-variant | ASB11 | GRCh38.p7 | X:15296656 | TTTATTAAAAGCTCG[C/T]TCATTTTGATAATTT | 140456 |
rs5935937 | snp | A/G | 0.489502 | 0.0716857 | intron-variant | ASB11 | GRCh38.p7 | X:15300243 | AAGATCATCTAGAGT[A/G]GATCACCTCAATTGT | 140456 |
rs5935938 | snp | C/T | 0.477263 | 0.10417 | intron-variant | ASB11 | GRCh38.p7 | X:15301214 | GTGATCCACCCACCT[C/T]GGCCTCCTAAAGTGC | 140456 |
rs5935939 | snp | A/G | 0.48872 | 0.0742474 | intron-variant | ASB11 | GRCh38.p7 | X:15301540 | AGACAGAGAGAGAGA[A/G]AGAAAGAAAAAGAGA | 140456 |
rs5935940 | snp | C/T | 0.49091 | 0.0668016 | intron-variant | ASB11 | GRCh38.p7 | X:15304823 | gaggttgcagtgagc[C/T]aagattatgccactg | 140456 |
rs5935941 | snp | A/G | 0.497499 | 0.0352757 | intron-variant | ASB11 | GRCh38.p7 | X:15307068 | CCATTTAAAAATAAA[A/G]ACAGGATTTAAGTGG | 140456 |
rs5935942 | snp | C/G | 0.491882 | 0.0631893 | intron-variant | ASB11 | GRCh38.p7 | X:15307221 | TCCCATTAGACTCAA[C/G]TCATATACACAACAT | 140456 |
rs5935943 | snp | C/T | 0.460503 | 0.134865 | intron-variant | ASB11 | GRCh38.p7 | X:15310982 | ATAAGAGCGAAACTC[C/T]AACTCAAAAAATAAA | 140456 |
rs5935944 | snp | A/G | 0.472357 | 0.11427 | synonymous-codon, intron-variant | ASB11 | GRCh38.p7 | X:15314436 | TCCGGACCTTCTGAT[A/G]CGTTCTGAAACTTCA | 140456 |
rs5935945 | snp | G/T | 0.460055 | 0.135562 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316062 | TTTTCTCTTAATTCT[G/T]AAGTTTATAGAGGAT | 140456 |
rs5935946 | snp | A/T | 0.460354 | 0.135097 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317047 | ATATTTCATGAATCA[A/T]CCTTCTCTAGTTGGG | 140456 |
rs5980146 | snp | C/G | 0.0183711 | 0.0940641 | intron-variant | ASB11 | GRCh38.p7 | X:15284208 | agtgagccgagatcg[C/G]gccactgcactccag | 140456 |
rs6527420 | snp | C/T | 0.352982 | 0.227804 | intron-variant | ASB11 | GRCh38.p7 | X:15285521 | CCAGGATATCCAGGT[C/T]TACAAATCCTAGTCC | 140456 |
rs6628932 | snp | A/G | 0.455909 | 0.141779 | intron-variant | ASB11 | GRCh38.p7 | X:15284267 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 140456 |
rs6628937 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15287407 | tctctgctcatcgca[A/T]cctccgcctcccagg | 140456 |
rs6628942 | snp | A/T | 0.48 | 0.0979796 | intron-variant | ASB11 | GRCh38.p7 | X:15290041 | AATAAATAAATAAAT[A/T]AATTAATTAAATAAC | 140456 |
rs6628943 | snp | G/T | 0.491264 | 0.0655128 | intron-variant | ASB11 | GRCh38.p7 | X:15290425 | ATATGGCCTGCAACA[G/T]TACTTTGGTTAGTCT | 140456 |
rs6628945 | snp | C/T | 0.480942 | 0.0957375 | intron-variant | ASB11 | GRCh38.p7 | X:15291559 | AAAAAATACAAAAAT[C/T]AGCTGGGCACTGTGA | 140456 |
rs6628949 | snp | A/G | 0.45384 | 0.144738 | intron-variant | ASB11 | GRCh38.p7 | X:15294018 | ACTCTAAAACTTAAA[A/G]TATAATAAAAAATAA | 140456 |
rs6628964 | snp | A/G | 0.489655 | 0.0711726 | intron-variant | ASB11 | GRCh38.p7 | X:15303736 | TTTCCTTACTGGTAA[A/G]ATGGAAATATAATAA | 140456 |
rs6628967 | snp | C/T | 0.491264 | 0.0655128 | intron-variant | ASB11 | GRCh38.p7 | X:15306238 | TAATGAACATATGCA[C/T]GTATGTGTCCTTATA | 140456 |
rs6628971 | snp | A/C | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15312282 | CAAAGAAGCTTAAAA[A/C]CCAAAACTAATAACA | 140456 |
rs6632183 | snp | C/T | 0.472271 | 0.114437 | intron-variant | ASB11 | GRCh38.p7 | X:15283844 | TTTAAGTTAATCTTC[C/T]AATGGTACTTGGATT | 140456 |
rs6632267 | snp | C/T | 0.4608 | 0.1344 | intron-variant | ASB11 | GRCh38.p7 | X:15307448 | CAGGCATTAGATTCT[C/T]ATAAAGAGAATGTAA | 140456 |
rs6632268 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15309147 | gtcttgaactcctga[C/T]ctcaagtgatccact | 140456 |
rs6653931 | snp | A/G | 0.359796 | 0.224599 | intron-variant | ASB11 | GRCh38.p7 | X:15292949 | GGAAATTGGAGTCAG[A/G]AAAGCATTCCGAAGT | 140456 |
rs7049370 | snp | A/G | 0.481149 | 0.0952383 | intron-variant | ASB11 | GRCh38.p7 | X:15285643 | AAGCTCGGATCTGCT[A/G]AGGAAGATCATAATT | 140456 |
rs7062793 | snp | G/T | 0.0126344 | 0.0784702 | intron-variant | ASB11 | GRCh38.p7 | X:15284952 | CCAAGGAGCATCCAT[G/T]AGATAGAAAGCTACC | 140456 |
rs7066009 | snp | C/T | 0.263 | 0.249662 | intron-variant | ASB11 | GRCh38.p7 | X:15311173 | AGATATCTAAAATAT[C/T]GTAATAAAACTGAGT | 140456 |
rs7881570 | snp | A/G | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:15279917 | caaaaaagtttttTC[A/G]tttaattttatttgg | 140456 |
rs11094674 | snp | A/C | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15307311 | CGTGTGATTTGGTTT[A/C]TATAAAGCAGCAGTC | 140456 |
rs12006793 | snp | C/T | 0.425108 | 0.17843 | intron-variant | ASB11 | GRCh38.p7 | X:15284068 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTGT | 140456 |
rs12006826 | snp | C/G | 0.0389457 | 0.134 | intron-variant | ASB11 | GRCh38.p7 | X:15284168 | gaggcaggagaatgg[C/G]gtgaacccgggaggc | 140456 |
rs12010915 | snp | G/T | 0.0317957 | 0.122012 | intron-variant | ASB11 | GRCh38.p7 | X:15304936 | aaataaacaataaga[G/T]attatatcttatcaa | 140456 |
rs12013880 | snp | A/T | 0.0317957 | 0.122012 | intron-variant | ASB11 | GRCh38.p7 | X:15309074 | gacacacatcaccac[A/T]cccagctaattttag | 140456 |
rs12401027 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15300902 | GAGAAGAGGTGGGTG[C/G]GAGACTGAGAGAGAA | 140456 |
rs12557809 | snp | G/T | 0.352406 | 0.228063 | intron-variant | ASB11 | GRCh38.p7 | X:15309585 | gtccatggagaaatt[G/T]tcttccatgaaacca | 140456 |
rs12687741 | snp | G/T | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281712 | ttttttttttttttg[G/T]tttgagacggagtct | 140456 |
rs12688765 | snp | G/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15292886 | GCCACCAAAACACCA[G/T]CAAAGAGGATCTGGA | 140456 |
rs12690160 | snp | A/G | 0.47326 | 0.112495 | intron-variant | ASB11 | GRCh38.p7 | X:15300905 | AAGAGGTGGGTGGGA[A/G]ACTGAGAGAGAAGAG | 140456 |
rs12834070 | snp | C/T | 0.291966 | 0.246453 | intron-variant | ASB11 | GRCh38.p7 | X:15284027 | ggaggccaaggtggg[C/T]ggatcacgaggtcag | 140456 |
rs12834451 | snp | C/G | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15284048 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 140456 |
rs12841882 | snp | A/G | 0.261904 | 0.249716 | intron-variant | ASB11 | GRCh38.p7 | X:15307716 | agtcaaaagcacccc[A/G]aggaggggtgaggac | 140456 |
rs12843347 | snp | A/G | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15302663 | CTCTGCTACAGCCAA[A/G]GCTAATAAAGAATGA | 140456 |
rs12843560 | snp | A/C | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15302698 | TAATTATAGCATAAG[A/C]ATGAAGGATCAAGTC | 140456 |
rs12843739 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15285137 | AGTTGGTATTTAATC[C/T]ttctttttttttttt | 140456 |
rs12843742 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15285141 | GGTATTTAATCtttc[C/T]ttttttttttttttt | 140456 |
rs12845370 | snp | A/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15296296 | aaaaaaaGAAAATGC[A/T]CGACCACAATGGCAT | 140456 |
rs12846060 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15312246 | AAGAAAAAAAAATAT[A/C]CATATAATAGACAAA | 140456 |
rs12846066 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15312257 | ATATACATATAATAG[A/C]CAAAATAAACAAAGA | 140456 |
rs12846074 | snp | A/C | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15312266 | TAATAGACAAAATAA[A/C]CAAAGAAGCTTAAAA | 140456 |
rs12851814 | snp | A/C | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15312356 | GTAATAGTTTAAGCC[A/C]CAAAGACATATAAAA | 140456 |
rs12859158 | snp | C/T | 0.374005 | 0.217078 | intron-variant | ASB11 | GRCh38.p7 | X:15301249 | ATTACAGGCGTGAGC[C/T]ACCACATCCGGCCAG | 140456 |
rs16979812 | snp | A/G | 0.0660089 | 0.169255 | intron-variant | ASB11 | GRCh38.p7 | X:15298525 | GGAAATGGAGCACCT[A/G]TGAAGTCTGCTAGGC | 140456 |
rs16979814 | snp | A/G | 0.0328205 | 0.123827 | intron-variant | ASB11 | GRCh38.p7 | X:15303771 | ATATTTGTCAAGTGC[A/G]TTGGTCTCTAAGTAG | 140456 |
rs34025595 | snp | C/T | 0.0104621 | 0.0715654 | missense | ASB11 | GRCh38.p7 | X:15287983 | GGTTAGCTCCATAGT[C/T]GGTTAGCAGGTGGAT | 140456 |
rs34057288 | in-del | -/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15297018 | TGGTACAAGGCCGGG[-/C]CGCGGTGGCTCACGC | 140456 |
rs34332247 | in-del | -/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15311660 | AGCTTAAAATAGCCC[-/T]TTTTTTTTTTTGAAA | 140456 |
rs34551144 | snp | A/G | 0.421791 | 0.181625 | intron-variant | ASB11 | GRCh38.p7 | X:15284080 | ACACGGTGAAACCCC[A/G]TGTCCACTAAAAATA | 140456 |
rs34660573 | in-del | -/T | | | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15315342 | AAGTATAAATATAAT[-/T]CTGCCTTCCAGAAAT | 140456 |
rs34670756 | in-del | -/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15288203 | TTTGAAAATATGCAA[-/C]CTCAAGCCTAGAACC | 140456 |
rs34708436 | in-del | -/CT/TC | | | intron-variant | ASB11 | GRCh38.p7 | X:15294883 | ATTTCCTATAAATTT[-/CT/TC]CTCTTAGTTCACGTC | 140456 |
rs34773033 | snp | C/T | 0.417974 | 0.185161 | intron-variant | ASB11 | GRCh38.p7 | X:15284085 | GTGAAACCCCGTGTC[C/T]ACTAAAAATACAAAA | 140456 |
rs34826963 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15284270 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA | 140456 |
rs35110928 | in-del | -/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15294686 | AACCCCCATTAAATT[-/G]GGAAAGTTAAAGATA | 140456 |
rs35413500 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15296574 | CTCAGTCACCCTTTG[-/A]AAAAAGTTTGGAGAT | 140456 |
rs35650807 | snp | A/T | 0.0714214 | 0.174956 | intron-variant | ASB11 | GRCh38.p7 | X:15290037 | TCAAAATAAATAAAT[A/T]AATTAATTAATTAAA | 140456 |
rs35762920 | in-del | -/AGTC | 0.382114 | 0.21224 | | | GRCh38.p7 | X:15276721 | TGTCTACATAGACAT[-/AGTC]AGATGGTTTATGGAT | 140456 |
rs35775215 | snp | C/T | 0.423873 | 0.179634 | | | GRCh38.p7 | X:15276461 | AGCTGGGACTACAGG[C/T]GCCCGCCAACACGCC | 140456 |
rs35859007 | snp | C/T | 0.0333887 | 0.124818 | missense | ASB11 | GRCh38.p7 | X:15287941 | CCAGATCAAGCGCAC[C/T]TTTGCCCTGAGCATT | 140456 |
rs36040626 | snp | C/G | 0.417974 | 0.185161 | intron-variant | ASB11 | GRCh38.p7 | X:15284082 | ACGGTGAAACCCCGT[C/G]TCCACTAAAAATACA | 140456 |
rs41309559 | snp | C/G | 0.0989831 | 0.199233 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283502 | TCCCAGGAACACTTA[C/G]GACTATTGGTATAGG | 140456 |
rs55651049 | snp | A/G | 0.127804 | 0.218101 | intron-variant | ASB11 | GRCh38.p7 | X:15300495 | TTTAACAGTGTATAA[A/G]AGTAAAGAAGTAGGG | 140456 |
rs56075342 | snp | A/G | 0.0312828 | 0.12109 | intron-variant | ASB11 | GRCh38.p7 | X:15304179 | TAAACTTGGTGAAAC[A/G]AAAATCCCAGCAAAA | 140456 |
rs56755333 | in-del | -/TTTC/TTTT | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281710 | CTTTTTTTTTTTTTT[-/TTTC/TTTT]GTTTTGAGACGGAGT | 140456 |
rs57166377 | snp | C/T | 0.0753365 | 0.178865 | | | GRCh38.p7 | X:15280232 | AGCCTCTAATAAGCA[C/T]AATTCTACTCTCTGT | 140456 |
rs57648100 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15297319 | CAAAACAAAAAAAAA[-/A]CATGGTACAATAAAG | 140456 |
rs57936733 | snp | C/T | 0.0821446 | 0.185269 | intron-variant | ASB11 | GRCh38.p7 | X:15314234 | ACACCAAAACTATTA[C/T]TGAAAATTTTAGAAA | 140456 |
rs58066751 | snp | C/T | 0.0307697 | 0.120159 | intron-variant | ASB11 | GRCh38.p7 | X:15302619 | TGCCTCGAATGGCAA[C/T]GGTGGGACCTGGATA | 140456 |
rs58244064 | snp | A/G | 0.0183711 | 0.0940641 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281793 | ATCTCCGCCTCCCGG[A/G]TTCAAGTGATTCTCC | 140456 |
rs58369541 | snp | C/T | 0.0979747 | 0.198465 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316724 | AGGTGATCCACCCAC[C/T]TTGGCCTCCCAAAGT | 140456 |
rs58595330 | in-del | -/CTTTAA | | | intron-variant | ASB11 | GRCh38.p7 | X:15312840 | TTTTAATACACCTAA[-/CTTTAA]ATATATTGTTATGGG | 140456 |
rs58628495 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15296268 | TGGAAAAAAAAAAAA[-/A]CAAAAAAAGAAAATG | 140456 |
rs58628655 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15291569 | AAAATCAGCTGGGCA[A/C]TGTGACAGGTGCCTG | 140456 |
rs59613554 | snp | A/C | 0.0699487 | 0.17344 | intron-variant | ASB11 | GRCh38.p7 | X:15297309 | CAAAACAAAACAAAA[A/C]AAAAAAAAAACATGG | 140456 |
rs60325648 | in-del | -/TG/TT | 4.97698e-05 | 0.00498823 | intron-variant | ASB11 | GRCh38.p7 | X:15314346 | TTTTTTTTTTTTTTT[-/TG/TT]GTAACTAGTCAAAGT | 140456 |
rs60517241 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | ASB11 | GRCh38.p7 | X:15283975 | GTGATACACGGGGCC[A/G]GGCACGGTGGCTCAC | 140456 |
rs60542067 | in-del | -/AAAA | | | intron-variant | ASB11 | GRCh38.p7 | X:15284267 | AAAAAAAAAAAAAAA[-/AAAA]GAAAGAAAGAAAGAA | 140456 |
rs60765469 | in-del | -/AAAAAA | | | intron-variant | ASB11 | GRCh38.p7 | X:15309991 | AAAAAAAAAAAAAAA[-/AAAAAA]GTAGAAGTCCTTTTT | 140456 |
rs60772918 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15292419 | TTGCTATCATCAAAA[-/A]TGTTGCTCTTTGGGT | 140456 |
rs60943921 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15305594 | AACAAGAAAAAAAAA[-/A]GATTAGATAGATAGA | 140456 |
rs61274740 | snp | A/C | 0.0353775 | 0.128208 | intron-variant | ASB11 | GRCh38.p7 | X:15297314 | CAAAACAAAACAAAA[A/C]AAAAACATGGTACAA | 140456 |
rs61756318 | snp | C/T | | | splice-donor-variant | ASB11 | GRCh38.p7 | X:15287880 | CCCAGCCCTTGGTTA[C/T]CTTCACGGAGCAAGA | 140456 |
rs62580241 | snp | A/C/G | 0.015263 | 0.0861605 | | | GRCh38.p7 | X:15276539 | AGCCAGGATGGTCTC[A/C/G]ATCTCCTGACCTCGT | 140456 |
rs66828848 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15312525 | AAAAAAAAAAAAAAA[-/A]GAGTGCTCTGGACCT | 140456 |
rs68119315 | in-del | -/A | 0.453356 | 0.145418 | intron-variant | ASB11 | GRCh38.p7 | X:15291727 | ATAAAAAAAAAATTT[-/A]AAAAAATTAAAAAAA | 140456 |
rs68134042 | snp | C/T | 0.261904 | 0.249716 | intron-variant | ASB11 | GRCh38.p7 | X:15307414 | GGTTTCAGGATGACA[C/T]TGTACCACCTCAGAT | 140456 |
rs72229384 | in-del | -/TCAG | | | | | GRCh38.p7 | X:15276723 | TCTACATAGACATAG[-/TCAG]ATGGTTTATGGATAG | 140456 |
rs73189534 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15294054 | AAAATAAATAAATAA[A/G]ATTAAAAGATTAAAT | 140456 |
rs73189537 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15295538 | GTTTCTTTCACCAGG[C/G]CTCTGAAACTAGGAA | 140456 |
rs73447232 | snp | A/G | 0.0343555 | 0.126481 | intron-variant | ASB11 | GRCh38.p7 | X:15286178 | AGGAAATCCTCAAGT[A/G]AACTGATATGCATGT | 140456 |
rs73447235 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15290326 | ATTACTCTGAAAAGC[C/T]AGTGCTCAAACCCAA | 140456 |
rs73447236 | snp | A/T | 0.0348667 | 0.127349 | intron-variant | ASB11 | GRCh38.p7 | X:15295490 | AAGAAATAAGATGAC[A/T]CTCAGGTTTGCAGCT | 140456 |
rs73635072 | snp | G/T | 0.0485612 | 0.148062 | | | GRCh38.p7 | X:15277956 | CTAATGCCACTATTT[G/T]GGGTTTATATGTCCT | 140456 |
rs73635073 | snp | A/G | 0.0173306 | 0.0914601 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282686 | CAATAAGCAATAGAT[A/G]CCAACCTCTGGGTGC | 140456 |
rs73635074 | snp | C/T | 0.0941651 | 0.195488 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282840 | ATATATAACTTTATA[C/T]ATAAAGAACTTTGAA | 140456 |
rs73635075 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | ASB11 | GRCh38.p7 | X:15284333 | GGAAGGACTGAACAC[A/G]CAGGACTCCAAGACA | 140456 |
rs73635076 | snp | A/G | 0.0338441 | 0.125605 | intron-variant | ASB11 | GRCh38.p7 | X:15285165 | TTTTTTTTTTTTGAC[A/G]GAATCTCACTCGGTC | 140456 |
rs73635077 | snp | A/G | 0.0338441 | 0.125605 | intron-variant | ASB11 | GRCh38.p7 | X:15285236 | AACCTCTGCCTCCCG[A/G]GTTTAGGCAGTTCTC | 140456 |
rs73635078 | snp | A/T | 0.0328205 | 0.123827 | intron-variant | ASB11 | GRCh38.p7 | X:15285239 | CTCTGCCTCCCGGGT[A/T]TAGGCAGTTCTCTGC | 140456 |
rs73635079 | snp | G/T | 0.0348667 | 0.127349 | intron-variant | ASB11 | GRCh38.p7 | X:15286277 | AAGGTATATATGATG[G/T]AGTGGTTTCACAAAA | 140456 |
rs73635080 | snp | A/T | 0.0323082 | 0.122924 | intron-variant | ASB11 | GRCh38.p7 | X:15301331 | TTAAAAATAATCAAA[A/T]CACATCCAATTTAAA | 140456 |
rs73635081 | snp | C/T | 0.0358881 | 0.129059 | intron-variant | ASB11 | GRCh38.p7 | X:15308820 | TCCACCTCCTCTTTA[C/T]AAATCAGGGGTCCCT | 140456 |
rs73635082 | snp | C/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15311541 | AGACAGGAAAAAGGA[C/T]TCAGAATGCTGAGTT | 140456 |
rs74366512 | snp | G/T | 0.5 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15306171 | TTAAATACCCATCAA[G/T]GATAGACTGGATAAT | 140456 |
rs74901064 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281698 | TCTTTCTTTCTTTCT[C/T]TTTTTTTTTTTTGTT | 140456 |
rs74919898 | in-del | -/TAGA | | | intron-variant | ASB11 | GRCh38.p7 | X:15305641 | AGATAGATAGATAGA[-/TAGA]ATCACTGGTGATCCC | 140456 |
rs75209491 | snp | G/T | 0.5 | 0 | | | GRCh38.p7 | X:15277604 | AACCGCAGGCAAAAT[G/T]GAAACTGAAGGGTTA | 140456 |
rs75385762 | snp | G/T | 0.5 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15286697 | AAAAGTGCACACTCT[G/T]GGGTCAGATGGCTCA | 140456 |
rs75949782 | snp | A/G | 0.5 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15306170 | TATATGCCTATCAAT[A/G]ATAGACTGGATAAAG | 140456 |
rs76058321 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281711 | CTTTTTTTTTTTTTT[G/T]TTTTGAGACGGAGTC | 140456 |
rs76439032 | snp | A/C | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15286667 | AGACTCCATCTCAAA[A/C]AAAAAAAAAAAAAAA | 140456 |
rs76727117 | snp | G/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15306187 | TTGATAGACATTTAG[G/T]TTGATTCCATGTTTT | 140456 |
rs77483933 | snp | C/T | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281692 | TTTCTTTCTTTCTTT[C/T]TTTCTTTTTTTTTTT | 140456 |
rs78006694 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281697 | TTCTTTCTTTCTTTC[C/T]TTTTTTTTTTTTTGT | 140456 |
rs78192815 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15306186 | AGACATGGAATCAAC[C/G]CAAATGCTCATCAGT | 140456 |
rs78441824 | snp | G/T | 0.5 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15311670 | TAGCCCTTTTTTTTT[G/T]TGAAAGAGGGCACTA | 140456 |
rs78996199 | in-del | -/ATGTATATACATACATGTAC | | | | | GRCh38.p7 | X:15275560 | TATATATGCATGTAC[-/ATGTATATACATACATGTAC]TTGTATATATGTGTG | 140456 |
rs79284344 | snp | C/G | 0.00791544 | 0.0624105 | intron-variant | ASB11 | GRCh38.p7 | X:15284992 | AAACAATCGATCTTA[C/G]TTAAAATCTTGGGAA | 140456 |
rs79649676 | snp | A/G | 0 | 0 | | | GRCh38.p7 | X:15276560 | CTGACCTCGTGATCC[A/G]CCCGCCGTGGCCTCC | 140456 |
rs111394800 | snp | A/C | 0.05658 | 0.158394 | intron-variant | ASB11 | GRCh38.p7 | X:15290283 | ATGGAAGTGACAAGA[A/C]CCAGAGGGACAAACG | 140456 |
rs111452972 | snp | C/T | 0 | 0 | missense | ASB11 | GRCh38.p7 | X:15283584 | CATGCTCGACCGAGA[C/T]ACTTCCGGACACACA | 140456 |
rs112078885 | snp | C/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15311662 | GCTTAAAATAGCCCT[C/T]TTTTTTTTTGAAAGA | 140456 |
rs112173368 | snp | A/C | 0.0555816 | 0.157167 | intron-variant | ASB11 | GRCh38.p7 | X:15294612 | CTGGGTTCAAATGAC[A/C]CTCCTGCCTCAGCCT | 140456 |
rs112312321 | snp | A/G | 0.460652 | 0.134633 | intron-variant | ASB11 | GRCh38.p7 | X:15309923 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 140456 |
rs112393052 | snp | C/T | 0.0353775 | 0.128208 | intron-variant | ASB11 | GRCh38.p7 | X:15297267 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 140456 |
rs112443803 | snp | A/G | 0.0585734 | 0.160798 | intron-variant | ASB11 | GRCh38.p7 | X:15284019 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 140456 |
rs112613990 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15310847 | ACAAAAATTAGCCAG[C/T]GTGGTGGCGGGCGCC | 140456 |
rs112696346 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15298488 | AGGCCTTGATTTCCA[A/G]ACAAGGAGGGCATGT | 140456 |
rs112771947 | snp | A/G | | | | | GRCh38.p7 | X:15277912 | CCTTCTGAATGTCAG[A/G]AGACCAAAAATGCCA | 140456 |
rs112876369 | snp | A/G | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15283716 | CTGGAAGAGGCGGAA[A/G]TTTTCTAAAAGCAGA | 140456 |
rs112980921 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15310628 | GATAAAAAACGATTA[A/C]ACTGTTTTTGTAATT | 140456 |
rs113052945 | snp | A/G | 0 | 0 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317218 | TATAGTTATACAAGT[A/G]GCCTAATAAATCTTA | 140456 |
rs113130220 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315668 | AGTTATAATTGGTAT[C/T]ATATGACATCTATTT | 140456 |
rs113376517 | in-del | -/TA | 0 | 0 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282976 | GTGTGTATATATATA[-/TA]CGTATATATATATAC | 140456 |
rs113419621 | snp | C/T | 0.0465453 | 0.14528 | intron-variant | ASB11 | GRCh38.p7 | X:15284023 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG | 140456 |
rs113621530 | snp | C/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15302404 | TCAGGACTGCTGGTG[C/T]TAATGCATGCTGGAA | 140456 |
rs113711652 | snp | A/G | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15286099 | CAACATCACGTGGGA[A/G]CCTGCTAGACATGCA | 140456 |
rs113722762 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15314076 | AAAAAAAAAAAAAAA[A/G]AAGAGTGCACTTAAT | 140456 |
rs114288068 | snp | A/G | 0.0460406 | 0.14457 | | | GRCh38.p7 | X:15275885 | TGATGTATTCCATAT[A/G]CAAATGGAATATATC | 140456 |
rs115210684 | snp | A/T | 0.0480577 | 0.147375 | | | GRCh38.p7 | X:15275405 | AATCGTTCATTTTTT[A/T]AATATATGGATATGT | 140456 |
rs115651927 | snp | G/T | 0.022522 | 0.1037 | intron-variant | ASB11 | GRCh38.p7 | X:15305076 | AGAATCAGCTTCAAC[G/T]CATCTCCCTGCAAAA | 140456 |
rs115829004 | snp | G/T | 0.0414859 | 0.13792 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283314 | TTTCTACTTGCCCCT[G/T]GGTTAATGAGAACAT | 140456 |
rs116261272 | snp | A/G | 0.0235569 | 0.105941 | intron-variant | ASB11 | GRCh38.p7 | X:15289039 | AGCATCTTCCTGGCA[A/G]GCATACCTAGATTTC | 140456 |
rs137906487 | snp | C/T | 4.58111e-05 | 0.00478576 | synonymous-codon | ASB11 | GRCh38.p7 | X:15288020 | CACATTGGACTGCCT[C/T]GCTGCAGCATGGAGT | 140456 |
rs138186480 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | ASB11 | GRCh38.p7 | X:15308989 | TGGTGCAATCTCAGC[C/T]TACTGCAACCTCTGC | 140456 |
rs138213704 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15308474 | TTCAGCAAGTTGTCT[C/G]TCTAAGCAGATTTCC | 140456 |
rs138296053 | snp | C/T | 0.00738971 | 0.0603345 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315938 | GCAGGGTTGGAAAGA[C/T]AGAAACTTCTTGGCT | 140456 |
rs138337611 | snp | A/G | 0.192797 | 0.243368 | | | GRCh38.p7 | X:15276586 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 140456 |
rs138453288 | snp | G/T | | | | | GRCh38.p7 | X:15317647 | TTTAAAACATGGCTG[G/T]CCTATGTTTTACACG | 140456 |
rs138511368 | snp | A/G | 0.0204488 | 0.0990265 | intron-variant | ASB11 | GRCh38.p7 | X:15285872 | TAGCTGGGCGTGGTG[A/G]CACGCGCCTGTAATC | 140456 |
rs138555157 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | ASB11 | GRCh38.p7 | X:15299929 | CTGCATCCTTGCTGT[A/G]GCCAGCAGCTGTGAT | 140456 |
rs138601078 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15295839 | TCAGCAGTCTGCCTG[A/T]GACTCCAGTCATCTA | 140456 |
rs138718927 | snp | A/G | 0.000388463 | 0.0139313 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315592 | AAGCCATAGAAAACA[A/G]GACCATCTTCCATTT | 140456 |
rs138884464 | snp | A/G | 0.00475684 | 0.0485365 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314639 | TAGATAAAGAATGAT[A/G]TAATCCTGGAACCCC | 140456 |
rs138889546 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | ASB11 | GRCh38.p7 | X:15305053 | AACTTAGAAATTGAA[A/G]AAATAATAGAATCAG | 140456 |
rs138921698 | snp | C/G | 0.00422943 | 0.0457911 | | | GRCh38.p7 | X:15277947 | CAGATCATGCTAATG[C/G]CACTATTTTGGGTTT | 140456 |
rs138942411 | snp | A/G | 0.000189982 | 0.00974449 | synonymous-codon | ASB11 | GRCh38.p7 | X:15283529 | TAGGAGGAATCGTTC[A/G]AGTGGCTCTGGCAGA | 140456 |
rs139015955 | snp | C/T | 0.0282 | 0.115346 | intron-variant | ASB11 | GRCh38.p7 | X:15305852 | CATGGGGGTTTGTTT[C/T]ACAGAGTATTTCATC | 140456 |
rs139060020 | snp | A/G | 0.0753365 | 0.178865 | | | GRCh38.p7 | X:15275198 | GCACAATAATGCAGG[A/G]ACATAAACAACAAGA | 140456 |
rs139106385 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | ASB11 | GRCh38.p7 | X:15287007 | CTGAAATTCAGAAGA[C/T]AACCAATTCAGAAGA | 140456 |
rs139245811 | snp | A/G | 0.0287145 | 0.11633 | intron-variant | ASB11 | GRCh38.p7 | X:15296655 | ATTTATTAAAAGCTC[A/G]CTCATTTTGATAATT | 140456 |
rs139349712 | snp | C/T | 0.0317957 | 0.122012 | intron-variant | ASB11 | GRCh38.p7 | X:15303379 | AAATCTCGTAAGTTT[C/T]ACGAAAATTTATGAA | 140456 |
rs139489358 | snp | C/T | 0.0430067 | 0.140192 | intron-variant | ASB11 | GRCh38.p7 | X:15311831 | TGTTTTATATTTCCA[C/T]CTAGTGTGAATACCT | 140456 |
rs139974533 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | ASB11 | GRCh38.p7 | X:15284753 | TTTTGGCTGCAATAC[C/T]AGTTGCACAGTCATT | 140456 |
rs140149804 | snp | C/T | 0.0271702 | 0.113344 | intron-variant | ASB11 | GRCh38.p7 | X:15306428 | AACTCTCTTTGAGGC[C/T]GGGTGCAGTGGCTCA | 140456 |
rs140259454 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15303932 | TCTGCAAACAAGACT[A/G]ACTAGTTTAAATGAG | 140456 |
rs140293526 | snp | A/C | 0.016289 | 0.0887646 | intron-variant | ASB11 | GRCh38.p7 | X:15300195 | ATCTCAGAATCCCTG[A/C]AATTGTAGAAATGTG | 140456 |
rs140429809 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15308771 | TTTCTCCTTATTCTC[A/G]TGGTAGATTGACTTG | 140456 |
rs140433192 | snp | C/G/T | 0.000276343 | 0.0117518 | missense | ASB11 | GRCh38.p7 | X:15289630 | GGATCTCCATGCACT[C/G/T]TCTGTGACCTGGTGG | 140456 |
rs140499306 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | ASB11 | GRCh38.p7 | X:15289345 | GAAGCAGGACTGAGA[A/G]ATACAGACACTCATT | 140456 |
rs140540923 | snp | A/G | 0.0276852 | 0.114351 | | | GRCh38.p7 | X:15276223 | ACCAAAATTAGAGAC[A/G]TTGGATTACATACCT | 140456 |
rs140626306 | snp | C/T | 9.41332e-05 | 0.00685986 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15314374 | AGTAACATACCTCCC[C/T]GAAATGTGTGACAAA | 140456 |
rs140674300 | snp | C/G/T | 0.000615137 | 0.0175276 | synonymous-codon, missense | ASB11 | GRCh38.p7 | X:15283576 | CTTGATGACATGCTC[C/G/T]ACCGAGACACTTCCG | 140456 |
rs140756593 | snp | A/C | 0.0100156 | 0.0700533 | intron-variant | ASB11 | GRCh38.p7 | X:15301991 | GACTTGTTGACTCAC[A/C]CCTAATGAGTAGAAT | 140456 |
rs140761816 | snp | A/C | 0.0276852 | 0.114351 | intron-variant | ASB11 | GRCh38.p7 | X:15299556 | TTTCTTATCAGACTT[A/C]AGGTCTGTGTTGATG | 140456 |
rs140814611 | snp | C/G | 0.0343555 | 0.126481 | intron-variant | ASB11 | GRCh38.p7 | X:15304847 | GCCACTGTACTCTGG[C/G]CTGGGTGACAAAAAG | 140456 |
rs141168950 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | ASB11 | GRCh38.p7 | X:15286613 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 140456 |
rs141242752 | snp | C/T | 0.000189982 | 0.00974449 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15297633 | CTCCAAGGCATGCCT[C/T]GTGGAGAGAAGACAC | 140456 |
rs141277897 | snp | C/T | 2.27907e-05 | 0.00337562 | missense | ASB11 | GRCh38.p7 | X:15283509 | AACACTTAGGACTAT[C/T]GGTATAGGAGGAATC | 140456 |
rs141295583 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15313124 | TATTTAGCGGCCAGG[A/C]ACAGGTGCTCACACC | 140456 |
rs141302282 | snp | C/T | 0.00422943 | 0.0457911 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283311 | TGGTTTCTACTTGCC[C/T]CTTGGTTAATGAGAA | 140456 |
rs141364379 | snp | G/T | 0.0121112 | 0.0768695 | intron-variant | ASB11 | GRCh38.p7 | X:15308358 | CTGTGGTGCCATCTT[G/T]CATTCCACCAAGAAA | 140456 |
rs141713387 | snp | C/T | 0.0276852 | 0.114351 | intron-variant | ASB11 | GRCh38.p7 | X:15295895 | GTCAGCTCATGGGTA[C/T]TGATGAAGGAAGGCT | 140456 |
rs142033679 | snp | G/T | 2.28363e-05 | 0.003379 | missense | ASB11 | GRCh38.p7 | X:15287955 | CTTTTGCCCTGAGCA[G/T]TTCTACGCTTCAGGT | 140456 |
rs142097387 | snp | G/T | 0.00737819 | 0.0602881 | upstream-variant-2KB, synonymous-codon | ASB11 | GRCh38.p7 | X:15315504 | ATAGAAATGGGTTAG[G/T]AGAGCCAAAAAAACT | 140456 |
rs142153515 | snp | C/T | 0.0753365 | 0.178865 | | | GRCh38.p7 | X:15275485 | TTATATATGTATATA[C/T]GTGTATACATTTGTA | 140456 |
rs142160812 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15310144 | ACAGTGGGGTCTCCT[A/G]CTTTTCTATCCTTGT | 140456 |
rs142502781 | snp | G/T | 0.10601 | 0.20437 | intron-variant | ASB11 | GRCh38.p7 | X:15294420 | CTGCTATCCAGGCTG[G/T]AGTGCAGTGTCATGA | 140456 |
rs142702549 | snp | A/G | 4.59897e-05 | 0.00479507 | missense | ASB11 | GRCh38.p7 | X:15293254 | GCAGCACATTGACAC[A/G]TGCAGCACTGCCGCT | 140456 |
rs142890288 | in-del | -/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15283720 | AAGAGGCGGAAATTT[-/T]CTAAAAGCAGAAGAG | 140456 |
rs142930214 | snp | C/T | 0.0068637 | 0.0581785 | | | GRCh38.p7 | X:15276608 | AGGCGTGAGCCACTG[C/T]GCCCAGCCTATTTTT | 140456 |
rs142962808 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | ASB11 | GRCh38.p7 | X:15298585 | CTTTTTAGAAGCTTA[C/T]TGGTAGCAGCATGGA | 140456 |
rs143206039 | snp | A/G | 0.0430067 | 0.140192 | intron-variant | ASB11 | GRCh38.p7 | X:15313702 | CCAGCTCCAGATTAA[A/G]TTCAAACCATGCTTA | 140456 |
rs143402682 | snp | C/T | 0.000662079 | 0.0181824 | upstream-variant-2KB, synonymous-codon | ASB11 | GRCh38.p7 | X:15315462 | TTCTGCTATCCTAGC[C/T]GCTTCTTTTCTATTT | 140456 |
rs143404299 | snp | C/T | 0.000882039 | 0.0209819 | upstream-variant-2KB, splice-donor-variant | ASB11 | GRCh38.p7 | X:15315424 | ATTCATGTACTTTTA[C/T]CTGAAATTCCACCAT | 140456 |
rs143448901 | snp | A/T | 0.0333324 | 0.12472 | intron-variant | ASB11 | GRCh38.p7 | X:15290045 | AATAAATAAATAAAT[A/T]AATTAAATAACCTAG | 140456 |
rs143492892 | snp | A/T | 0.00939459 | 0.0678899 | missense | ASB11 | GRCh38.p7 | X:15289537 | TCACACAGTCTACCC[A/T]CTGGTAGGTGCAGGC | 140456 |
rs143624829 | snp | A/G | 0.00528398 | 0.051128 | | | GRCh38.p7 | X:15275891 | ATTCCATATACAAAT[A/G]GAATATATCCATGCA | 140456 |
rs143896253 | snp | C/G | 0.0235569 | 0.105941 | intron-variant | ASB11 | GRCh38.p7 | X:15306649 | TGGAGGCTGCAGTGA[C/G]CCAAGATCACGCCAT | 140456 |
rs144086386 | snp | A/G | 0.0580755 | 0.160203 | intron-variant | ASB11 | GRCh38.p7 | X:15285937 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 140456 |
rs144179935 | snp | A/G | 0.0525796 | 0.153379 | intron-variant | ASB11 | GRCh38.p7 | X:15284905 | ATGGACTGCATATGC[A/G]AATAGCCAGGTTAAC | 140456 |
rs144215885 | snp | C/T | 0.00738971 | 0.0603345 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316663 | TATTTTTAGTAGAGA[C/T]GAGGTTTCGCCATGT | 140456 |
rs144384274 | snp | C/T | 0.00016452 | 0.00906824 | synonymous-codon | ASB11 | GRCh38.p7 | X:15293195 | TGCCTCATGGATGGG[C/T]GAGGCCAGGTGCACC | 140456 |
rs144407577 | snp | C/G | 0.0505727 | 0.150761 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316204 | TGAGGTCAGGAGTTT[C/G]CGACCAGCCTGGCCA | 140456 |
rs144425701 | snp | C/T | 0.00581083 | 0.0535878 | | | GRCh38.p7 | X:15275493 | GTATATATGTGTATA[C/T]ATTTGTATATGCATA | 140456 |
rs144572145 | snp | A/G | 0.00152209 | 0.027545 | missense | ASB11 | GRCh38.p7 | X:15293196 | GCCTCATGGATGGGC[A/G]AGGCCAGGTGCACCT | 140456 |
rs144616174 | snp | A/G | 0.0199298 | 0.0978146 | intron-variant | ASB11 | GRCh38.p7 | X:15299887 | AACTCCTACTTACAC[A/G]GCCACCATCTCCTGC | 140456 |
rs144624458 | in-del | -/CTTTAA | | | intron-variant | ASB11 | GRCh38.p7 | X:15312835 | TTGATTTTTAATACA[-/CTTTAA]CCTAAATATATTGTT | 140456 |
rs144683239 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15293464 | TTACAGTATTATGAA[A/G]CCTCATGAAGTTATT | 140456 |
rs144785064 | snp | C/T | 0.0748481 | 0.178387 | intron-variant | ASB11 | GRCh38.p7 | X:15297473 | TAGAACCAGCCCAGC[C/T]CTTACCCACAGTGGG | 140456 |
rs144848134 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15294562 | ATTATTTGTAGACAG[C/T]GTCTAGCTATCTTGC | 140456 |
rs144863246 | snp | A/C | 0.0302564 | 0.119217 | | | GRCh38.p7 | X:15278609 | GCTTAACACAGTACT[A/C]AGACATTCAGCAAGA | 140456 |
rs145057594 | snp | A/G | 4.55773e-05 | 0.00477353 | missense | ASB11 | GRCh38.p7 | X:15283519 | ACTATTGGTATAGGA[A/G]GAATCGTTCGAGTGG | 140456 |
rs145125518 | snp | C/G | 0.0121112 | 0.0768695 | | | GRCh38.p7 | X:15275373 | CTGGTGAAGGATCAT[C/G]ATGCCCACAACTTAC | 140456 |
rs145130914 | snp | C/G | 0.0199298 | 0.0978146 | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281578 | ATTAGCCATATGTAG[C/G]TAGCAGCTACTGTAT | 140456 |
rs145254572 | snp | C/G | 0.0630423 | 0.165972 | intron-variant | ASB11 | GRCh38.p7 | X:15313163 | CAGCACTTTGGGAGG[C/G]CAAGGTGGGCAGATC | 140456 |
rs145391252 | snp | G/T | 0.00633741 | 0.0559334 | intron-variant | ASB11 | GRCh38.p7 | X:15303564 | ATTTTTCAGACAATT[G/T]AATCTCCCAAAAGTT | 140456 |
rs145428689 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | ASB11 | GRCh38.p7 | X:15294222 | TCGGGAACCGCAGGA[A/G]TGGTAGGGAGCCTCT | 140456 |
rs145651470 | snp | A/G | 0.00528398 | 0.051128 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282661 | AAATAACAGCATTTA[A/G]TATCAGAAGCAATAA | 140456 |
rs145809121 | snp | G/T | 0.00634102 | 0.0559491 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15297667 | GTTAATTGTCACAAG[G/T]TTCACATTGACACCC | 140456 |
rs145832401 | snp | A/G | 0.000524025 | 0.0161783 | missense | ASB11 | GRCh38.p7 | X:15283591 | GACCGAGACACTTCC[A/G]GACACACAGGCGGCA | 140456 |
rs145982537 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15290696 | CCTAAAAAATCATGT[C/T]ATTACTAATTAATTT | 140456 |
rs146003151 | snp | C/G | 0.0131573 | 0.0800346 | intron-variant | ASB11 | GRCh38.p7 | X:15287248 | CAATATTACAAAGCA[C/G]AGTTTTGGTTTGCTC | 140456 |
rs146244200 | snp | C/T | 0.0235569 | 0.105941 | intron-variant | ASB11 | GRCh38.p7 | X:15295998 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG | 140456 |
rs146811336 | snp | C/T | 2.32186e-05 | 0.00340716 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15297680 | AGGTTCACATTGACA[C/T]CCTATAATTTAGAAA | 140456 |
rs147005387 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15308416 | TCCCTCACCACATTG[C/T]TGCTTTCCAATTCTC | 140456 |
rs147022897 | snp | A/G | 0.0240739 | 0.107039 | intron-variant | ASB11 | GRCh38.p7 | X:15305506 | GAATGGAGTCTCTGG[A/G]TGAAGAGAAGCAGGA | 140456 |
rs147157187 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15279264 | AAAATGCACAAGGTA[C/T]CATATACATTTTAGA | 140456 |
rs147170563 | snp | A/G | 0.000274038 | 0.0117023 | synonymous-codon | ASB11 | GRCh38.p7 | X:15289541 | ACAGTCTACCCTCTG[A/G]TAGGTGCAGGCCACA | 140456 |
rs147370458 | snp | C/G | 0.0650211 | 0.168175 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316683 | TTTCGCCATGTTGGC[C/G]AGGCTGGTCTCGAAC | 140456 |
rs147612155 | snp | A/G | 0.0404706 | 0.136372 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317473 | GAGCTTATATTACCT[A/G]GTAGAATGCCAGTGT | 140456 |
rs147628516 | snp | C/G | 0.0271702 | 0.113344 | intron-variant | ASB11 | GRCh38.p7 | X:15313323 | AGAATTGCTTGAACC[C/G]CAGAGGAGGAGGTTG | 140456 |
rs147719021 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15289382 | GAGAAGTTTTGTTTT[C/T]AGCATTCAAACATAA | 140456 |
rs147807558 | snp | A/C | 0.0630423 | 0.165972 | intron-variant | ASB11 | GRCh38.p7 | X:15312958 | GGGTTTTGAATAAAG[A/C]GTTGTTATTTTTTAA | 140456 |
rs147823772 | snp | A/G | 0.0348667 | 0.127349 | intron-variant | ASB11 | GRCh38.p7 | X:15307953 | CTCTTCACAGCTCCT[A/G]GCCTTTTCCCACTCC | 140456 |
rs147841089 | in-del | -/TAACTT | | | intron-variant | ASB11 | GRCh38.p7 | X:15312838 | ATTTTTAATACACCT[-/TAACTT]AAATATATTGTTATG | 140456 |
rs147971829 | snp | C/T | 4.82521e-05 | 0.00491159 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315439 | CCTGAAATTCCACCA[C/T]AGATCTCTTCTGCTA | 140456 |
rs148049394 | snp | A/G | 0.0748481 | 0.178387 | intron-variant | ASB11 | GRCh38.p7 | X:15296168 | GCAGGGGAATCGTTC[A/G]AATCTAGGAAGTGGA | 140456 |
rs148086085 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | ASB11 | GRCh38.p7 | X:15313721 | AAACCATGCTTACAT[A/G]GGTTTTGACTATAAG | 140456 |
rs148298291 | snp | A/T | 0.00528398 | 0.051128 | | | GRCh38.p7 | X:15276001 | TGTGGTTATTCAGCG[A/T]TTCATCCCTCACCAT | 140456 |
rs148381463 | snp | C/T | 0.00422943 | 0.0457911 | | | GRCh38.p7 | X:15278383 | GACATCGGCACCACT[C/T]TAGGATTCAGGGACC | 140456 |
rs148478852 | snp | A/G | 2.29896e-05 | 0.00339032 | synonymous-codon | ASB11 | GRCh38.p7 | X:15293249 | CTCCAGCAGCACATT[A/G]ACACATGCAGCACTG | 140456 |
rs148608360 | snp | A/G | 0.0183711 | 0.0940641 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316610 | CTCCCAAGAAGCTGG[A/G]ATTACAGGCATGCGT | 140456 |
rs149039963 | snp | A/G | 0.0748481 | 0.178387 | intron-variant | ASB11 | GRCh38.p7 | X:15295391 | TAGATGACTATGGGA[A/G]TAGGATAAAGGAGAG | 140456 |
rs149062445 | snp | C/T | 0.0404706 | 0.136372 | intron-variant | ASB11 | GRCh38.p7 | X:15307715 | GAGTCAAAAGCACCC[C/T]GAGGAGGGGTGAGGA | 140456 |
rs149114115 | snp | A/C | 0.0110639 | 0.0735497 | intron-variant | ASB11 | GRCh38.p7 | X:15313693 | ATTTGTATTCCAGCT[A/C]CAGATTAAATTCAAA | 140456 |
rs149205453 | snp | C/T | 4.57765e-05 | 0.00478395 | synonymous-codon, intron-variant | ASB11 | GRCh38.p7 | X:15314442 | CCTTCTGATACGTTC[C/T]GAAACTTCACAATTC | 140456 |
rs149359214 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | ASB11 | GRCh38.p7 | X:15305986 | CGTGTCCATGTGTTC[C/T]CATCATTTAGCTCCA | 140456 |
rs149519656 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | ASB11 | GRCh38.p7 | X:15300522 | AGGGGTGTAAAAGAA[A/G]AAGTTGAACTTTTGT | 140456 |
rs149687408 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15312797 | TTTCTGGTTTGAGTT[A/T]AACACTTCCACAAAA | 140456 |
rs149882464 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15311925 | AGTGCTGTGCAATAG[A/G]CAGTATGCACATTGT | 140456 |
rs149951868 | snp | G/T | 0.00528398 | 0.051128 | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281460 | GAAAACAAAACAAAG[G/T]TCATAATGTTTCATA | 140456 |
rs149964252 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15284243 | GGCGACAGAGCGAGA[C/T]TCCGCCTCAAAAAAA | 140456 |
rs150507780 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | ASB11 | GRCh38.p7 | X:15311549 | AAAAGGATTCAGAAT[A/G]CTGAGTTAGGCAGAG | 140456 |
rs150596588 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15296410 | TGTCATTAAGCACTT[A/G]AAAACATTGCAGCTC | 140456 |
rs150667346 | snp | A/G | 0.00370173 | 0.0428621 | | | GRCh38.p7 | X:15277406 | TGTCTGTCTTTCACA[A/G]TGTTCTACAGTGTCT | 140456 |
rs150669378 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15306401 | TTGAAAGCTGACAAG[C/T]AGAATATTTTAAACT | 140456 |
rs150736778 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15286782 | CTTTTCCCATTTGTA[C/G]CTGGCATAGCAACCA | 140456 |
rs150858220 | snp | C/T | 0.0292288 | 0.117303 | intron-variant | ASB11 | GRCh38.p7 | X:15302944 | ATCACGCATCAGGCT[C/T]TCTCGTCAGCCACTT | 140456 |
rs150900542 | snp | C/G | 0.022522 | 0.1037 | intron-variant | ASB11 | GRCh38.p7 | X:15283739 | AAAGCAGAAGAGAAG[C/G]TGGATCTGTATAGGA | 140456 |
rs151024633 | snp | C/T | 4.6005e-05 | 0.00479587 | missense | ASB11 | GRCh38.p7 | X:15293257 | GCACATTGACACATG[C/T]AGCACTGCCGCTGCA | 140456 |
rs151193420 | snp | C/T | 0.00317376 | 0.039709 | | | GRCh38.p7 | X:15280314 | GTTTATCTTTCTGTG[C/T]GTGACTTACTTAACA | 140456 |
rs151266813 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15289238 | TTTCTTGCTGCGTAT[A/G]GATAAGGAGGGCTGT | 140456 |
rs180749943 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15290588 | GACATGATAAATTTG[C/T]AACCTGTGAATGCTT | 140456 |
rs180759585 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15277293 | CTCTTTAATCTGCTT[C/T]ATTTTTCTTTTTATC | 140456 |
rs180771374 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15308992 | TGCAATCTCAGCTTA[C/T]TGCAACCTCTGCCTC | 140456 |
rs180988234 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15286054 | TCTAGACCAGTGGTA[C/T]GCAAAGTGTGGTCCT | 140456 |
rs180991004 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15313604 | ATACTATGCTACTTG[C/T]AAATTAACCTATTTT | 140456 |
rs181003338 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305912 | TTATTTTTCCTGATC[C/G]TCTCACTCCTCCTAC | 140456 |
rs181032365 | snp | A/C | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15275888 | TGTATTCCATATACA[A/C]ATGGAATATATCCAT | 140456 |
rs181043952 | snp | C/T | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:15280272 | CTCAATTTTTTTAGC[C/T]TCCACATGTAAGCAA | 140456 |
rs181045050 | snp | A/C/G | 2.45429e-05 | 0.00350298 | missense, synonymous-codon | ASB11 | GRCh38.p7 | X:15297574 | AGGGGCAGTACTCAC[A/C/G]TGTGCACCATTTTCC | 140456 |
rs181281079 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305351 | GTGCACCAACCCAAA[A/C]TGAGGGGACATTTTA | 140456 |
rs181303023 | snp | C/T | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15280077 | TCTCTTCTAGGTTTT[C/T]GAAAATACATAATAA | 140456 |
rs181379002 | snp | A/G | 0.0276852 | 0.114351 | intron-variant | ASB11 | GRCh38.p7 | X:15285423 | GGATTACAGGTGTGA[A/G]CCACCGCGCCCAGCC | 140456 |
rs181439075 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15305226 | CATCTGATGGAATGC[A/G]ATGAGCAACATCATG | 140456 |
rs181464214 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | ASB11 | GRCh38.p7 | X:15285181 | GAATCTCACTCGGTC[A/G]CCCAGGCTGAAATGC | 140456 |
rs181522045 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15313976 | AGAATTGCTTCAACC[A/G]GGACCTGGGAGGCGG | 140456 |
rs181621382 | snp | G/T | 0.00370173 | 0.0428621 | | | GRCh38.p7 | X:15280445 | TATCCATTGATCTGT[G/T]GACAGACATTTAAGT | 140456 |
rs181651373 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15302642 | CCTGGATAGGGTGAG[C/G]CACACCTCTGCTACA | 140456 |
rs181698059 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297979 | GAGCCTAAAGACAGC[A/G]TGACAGCCTCACATT | 140456 |
rs181877207 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15290011 | CCTGGCCGACAAAGC[A/G]AGACTCTGTCTCAAA | 140456 |
rs181909481 | snp | A/G | 0.0152462 | 0.0859689 | intron-variant | ASB11 | GRCh38.p7 | X:15283979 | TACACGGGGCCAGGC[A/G]CGGTGGCTCACGCCT | 140456 |
rs181936570 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15309828 | AAAAAATTAGCCAGG[C/T]GTGGTGGCGGGCGCC | 140456 |
rs182064731 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15311773 | ATGCAAACTTGTTTA[G/T]CAGCAAAGCATGGCC | 140456 |
rs182098060 | snp | A/T | 0 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15294843 | TTCATCCTCACCCTC[A/T]GTCTAGGAAGTTGTC | 140456 |
rs182134321 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15277543 | AAAAAAACATCCCAT[A/G]TAGTGTAAAAAGTGA | 140456 |
rs182163237 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | ASB11 | GRCh38.p7 | X:15308315 | CCCCAACTCTGATCC[A/T]GTGCCTCTGAGATCA | 140456 |
rs182164492 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | ASB11 | GRCh38.p7 | X:15301495 | ATAAATGAAAAATAC[A/G]TACACATGCACACAC | 140456 |
rs182189504 | snp | A/G | 0.194455 | 0.243752 | | | GRCh38.p7 | X:15276729 | TAGACATAGTCAGAT[A/G]GTTTATGGATAGGCA | 140456 |
rs182397576 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317577 | CATTTAGTCATGTCA[G/T]ACCAGTGATGTACAT | 140456 |
rs182418067 | snp | C/T | 0.5 | 0 | intron-variant | ASB11 | GRCh38.p7 | X:15291903 | AGCCAATTGTGGTGG[C/T]GGGCACCTGTAATCC | 140456 |
rs182460244 | snp | C/T | 0.372136 | 0.218135 | intron-variant | ASB11 | GRCh38.p7 | X:15284077 | CTAACACGGTGAAAC[C/T]CCGTGTCCACTAAAA | 140456 |
rs182509376 | snp | A/G | 0.00528398 | 0.051128 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314595 | GACTATTTTGAAAGA[A/G]AATCCTGGATGCAAA | 140456 |
rs182512859 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15299397 | TAGACAGATTGAAAA[A/T]TTTTCTGATTGGCAA | 140456 |
rs182544357 | snp | A/C | 0.00528398 | 0.051128 | | | GRCh38.p7 | X:15280973 | GAAGAGGCAGGTGGA[A/C]CAGTTGAGGTCAGGA | 140456 |
rs182657816 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15302878 | TCCATGCTGCCCACC[A/C]ACTGTGAGAGGAGGT | 140456 |
rs182678519 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299586 | GTTAAATTCTGGTCA[C/T]CTTTTCCTGAGTTCC | 140456 |
rs182886971 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282395 | ATGAGAAGAAGGAGA[A/G]GACAGAAAAGGAGAA | 140456 |
rs182898999 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15286580 | TGAGGCAGAAAAATC[A/G]CTTGAACCCGGGAGG | 140456 |
rs182913314 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15306659 | AGTGAGCCAAGATCA[C/T]GCCATTGCACTCCAG | 140456 |
rs182952806 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15306918 | GCACTGGGGTTGGTA[A/G]GACAGTCTTTACCCA | 140456 |
rs182968884 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15315057 | TTCTATTTCCTGAGA[G/T]AATTTAGTCTGGTTA | 140456 |
rs182977327 | snp | A/G | 0.0323082 | 0.122924 | | | GRCh38.p7 | X:15276411 | AAGCTCCGCCTCCCG[A/G]GTTCACGCCATTCTC | 140456 |
rs182990677 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281784 | CTTACTGCAATCTCC[A/G]CCTCCCGGGTTCAAG | 140456 |
rs183142940 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15303803 | CCAATCAAATACAAC[C/T]GCGATGTTAAGTGCT | 140456 |
rs183258456 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315964 | TGGCTTCCACAGAAA[C/T]AAAGCAAGTTATTTG | 140456 |
rs183272022 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15287626 | CACCACGCCCAGCCG[A/G]TTTTCTGGTTATTTT | 140456 |
rs183364991 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15303136 | TAAGGCAAAATGAAG[G/T]GCCAAGAAAGTCAAT | 140456 |
rs183490355 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15300491 | ATTTTTTAACAGTGT[A/G]TAAGAGTAAAGAAGT | 140456 |
rs183513245 | snp | A/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15276250 | ACCTAAACATTTAAA[A/T]AATTTAAGGAATTTA | 140456 |
rs183579797 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15293435 | TGGTGAATAAGTGAG[A/G]GAACTCCACATCTTT | 140456 |
rs183604176 | snp | C/T | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15280157 | ATTTCTTCTATCCAA[C/T]TATAATTTTGTATCC | 140456 |
rs183614805 | snp | A/C | 0.0204488 | 0.0990265 | intron-variant | ASB11 | GRCh38.p7 | X:15313480 | GTGTATATGTATACA[A/C]ACACACACACACATA | 140456 |
rs183618417 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297236 | AGAGCTTGCAGTGAG[C/T]GGAGATTGTGCCACT | 140456 |
rs183692236 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15307288 | GCCAGACACAAAAGA[A/T]CATGTACCGTGTGAT | 140456 |
rs183729668 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15288983 | TACTGTAGCAGGATA[A/G]ATATAAACTAGCCTG | 140456 |
rs183732944 | snp | A/G | 0.0640323 | 0.167081 | | | GRCh38.p7 | X:15276528 | TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 140456 |
rs183776102 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15310563 | AACCGTATATATTTC[A/T]ATAACATTGGTTCAG | 140456 |
rs183791259 | snp | A/G | 0.00422943 | 0.0457911 | | | GRCh38.p7 | X:15277696 | TTTTTTCATGAAGCT[A/G]AAGGCTACAGTAGTT | 140456 |
rs183836445 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15312820 | CCACAAAATTTTGTT[C/G]TTGATTTTTAATACA | 140456 |
rs184016708 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15295570 | CCAAGATGAGGAGCA[G/T]GTCCCAGAGGGAAGA | 140456 |
rs184143372 | snp | A/G | 0.00317376 | 0.039709 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316624 | GGATTACAGGCATGC[A/G]TCACCACGCCTGGAT | 140456 |
rs184147671 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15300784 | GGGTACAGTGTATAT[A/G]GGAACTGTCTGTATC | 140456 |
rs184158685 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284718 | AGAGTCCAGAATATG[C/G]TTGAATAGGATGAAT | 140456 |
rs184171933 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15307384 | TTTTTCCACAGATGA[A/G]GGTGGGCAGGGGATG | 140456 |
rs184287988 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15304393 | TGGATTGATATTGGA[A/G]CAATTAGCATGAAAA | 140456 |
rs184383020 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305291 | CACCGCTTCTGTGAT[A/G]TTTCTGCCCAAAATG | 140456 |
rs184436547 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15301173 | TCACCATGTTGCCCA[A/G]GCTGGTCTCGAACTC | 140456 |
rs184534591 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317160 | TTCTTGGCTATGTTC[A/G]ATTTTGTAAATTTTA | 140456 |
rs184549491 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283264 | CTTCACAGTTCTTTT[A/C]AGTTTCTTAACAACA | 140456 |
rs184640537 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15304618 | GCTGGCCAGGCTCAC[A/G]CCTGTAATCCCAGCA | 140456 |
rs184645671 | snp | C/T | 0.00317376 | 0.039709 | | | GRCh38.p7 | X:15279916 | GCAAAAAAGTTTTTT[C/T]GTTTAATTTTATTTG | 140456 |
rs184674352 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284976 | AGCTACCTGGAGGAC[A/C]AAACAATCGATCTTA | 140456 |
rs184692352 | snp | A/T | 0.0131573 | 0.0800346 | intron-variant | ASB11 | GRCh38.p7 | X:15308794 | TTGACTTGTCTTGGG[A/T]TGCTCTGACATCCAC | 140456 |
rs184711209 | snp | A/T | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15276964 | AATAATTTAAGTATC[A/T]AACAATATGGAAATA | 140456 |
rs184816941 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15290033 | TGTCTCAAAATAAAT[A/T]AATAAATAAATTAAT | 140456 |
rs184984172 | snp | A/G | 2.28271e-05 | 0.00337832 | synonymous-codon | ASB11 | GRCh38.p7 | X:15289547 | TACCCTCTGGTAGGT[A/G]CAGGCCACATATAGG | 140456 |
rs185244847 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15296091 | ATTACTGCACTAAAA[A/T]TACAAAAATTAGCTG | 140456 |
rs185365277 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15291305 | AAATATAATCAGTCA[A/C/G]GCACTGCAGACATAC | 140456 |
rs185373949 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15285229 | TCACTCCAACCTCTG[C/T]CTCCCGGGTTTAGGC | 140456 |
rs185374916 | snp | C/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15277338 | TATTATATTTGTATT[C/G]TTTATTCCCTGTTGT | 140456 |
rs185377754 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15309306 | TGGCACTAGATTCTT[A/G]GAAGAGTGTGAACTG | 140456 |
rs185379021 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15302680 | CTAATAAAGAATGAT[A/G]TGTAATTATAGCATA | 140456 |
rs185384174 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15313117 | AAAGACTTATTTAGC[A/G]GCCAGGCACAGGTGC | 140456 |
rs185546254 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15278853 | CTATTTATTTGTATG[C/T]TATTTGATAAGTTTA | 140456 |
rs185625297 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314648 | AATGATGTAATCCTG[A/G]AACCCCTGCAAACAC | 140456 |
rs185625585 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15299423 | GGCAATTGGTTGAAA[A/G]AGTTATTATCAATAG | 140456 |
rs185662577 | snp | C/T | 0.00528398 | 0.051128 | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281350 | GTGGCTAGTAGCTAC[C/T]GTATTGAATAGCACA | 140456 |
rs185688436 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15283980 | ACACGGGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 140456 |
rs185903573 | snp | C/T | | | | | GRCh38.p7 | X:15275535 | ACATGCCTGTATATG[C/T]ATATGTGTGTATATA | 140456 |
rs185931829 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15298073 | TCAAAACTTATGACA[C/T]GGGTCTCTCTTCTCC | 140456 |
rs185939568 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15280470 | TTAAGTTGATTTCAT[A/G]TCTTGCTTTTCTGAA | 140456 |
rs185985281 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15303010 | ACGGTTTGGTGGTGC[A/G]TGCCAAGAGAAGGAA | 140456 |
rs186120512 | snp | C/T | 0.0748481 | 0.178387 | intron-variant | ASB11 | GRCh38.p7 | X:15284144 | ATAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 140456 |
rs186363237 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15286075 | GTGTGGTCCTCAGAC[C/T]AGCACCATCAACATC | 140456 |
rs186377577 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306168 | TTCTTTACCCAGTCT[A/G]TCATTGATGGGCATT | 140456 |
rs186390800 | snp | A/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15275960 | CGTGAAGTCCTGCAG[A/T]GTGGAGAGCATCCTC | 140456 |
rs186442466 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15301561 | GAAAAAGAGAGAGAG[A/C]GAGCAGTGCACCCAG | 140456 |
rs186523095 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15285428 | ACAGGTGTGAGCCAC[C/G]GCGCCCAGCCAGTAT | 140456 |
rs186657568 | snp | A/T | 0.00738971 | 0.0603345 | intron-variant | ASB11 | GRCh38.p7 | X:15312241 | TAAAAAAGAAAAAAA[A/T]ATATACATATAATAG | 140456 |
rs186662404 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15295036 | AGACAAATACAAAAA[G/T]AATTTTTTTTAATTT | 140456 |
rs186691935 | snp | A/T | 0.00211696 | 0.0324653 | | | GRCh38.p7 | X:15278371 | CATAAATTGTAAGAC[A/T]TCGGCACCACTCTAG | 140456 |
rs186759995 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305529 | AAGCAGGAATTTTTT[G/T]GTACTGTTCTTGTAA | 140456 |
rs186992638 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15314044 | GCCTAGGCTACAGAG[C/G]GAGACTCCATCTCAA | 140456 |
rs187065872 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15304373 | TTGAATGCACTTTAC[A/G]AGGTTGGATTGATAT | 140456 |
rs187104453 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15313614 | ACTTGCAAATTAACC[C/T]ATTTTAAGAGATTGA | 140456 |
rs187121949 | snp | C/T | 0.00211696 | 0.0324653 | | | GRCh38.p7 | X:15280302 | AGAACATATGGTGTT[C/T]ATCTTTCTGTGCGTG | 140456 |
rs187159440 | snp | A/C | 0.0307697 | 0.120159 | | | GRCh38.p7 | X:15276470 | TACAGGCGCCCGCCA[A/C]CACGCCTGGCTAATT | 140456 |
rs187336193 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297820 | GGATTTCAAGTGCAA[C/G]CCACCAAGCCCAGCA | 140456 |
rs187416519 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15293090 | AGGGTCACCCTTGAA[A/T]GACTAACACTAGACC | 140456 |
rs187520753 | snp | G/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282605 | GTGGGTTCAGGTTGT[G/T]GGGGACACCCAGTGT | 140456 |
rs187526901 | snp | G/T | 0.0317957 | 0.122012 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316432 | AAAAAAAAAGACAAT[G/T]TACCCTAAAGCTGTA | 140456 |
rs187531550 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15300550 | TGTATAAAGAATGCC[C/T]CCTTACACATTTAAC | 140456 |
rs187586083 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15307294 | CACAAAAGAACATGT[A/G]CCGTGTGATTTGGTT | 140456 |
rs187607346 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15304474 | AGATGTGCGTATATA[C/T]GTATTTTTTTTTAGC | 140456 |
rs187659607 | snp | A/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15277561 | GTGTAAAAAGTGAAA[A/T]AATCTGTATTAGTAT | 140456 |
rs187668974 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | ASB11 | GRCh38.p7 | X:15310262 | TTGGGAGTTTTTCCA[A/T]TCCCTTCAGGAAGTA | 140456 |
rs187885034 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284729 | TATGGTTGAATAGGA[C/T]GAATGAGCTTTTGGC | 140456 |
rs188045497 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15284212 | AGCCGAGATCGGGCC[A/G]CTGCACTCCAGCCTG | 140456 |
rs188059017 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15303329 | TATACTAACACTAAC[A/G]ATATCTGATGAGCTA | 140456 |
rs188147009 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15287822 | AAATGCTACAGATGA[A/G]ACAGGAAGGGGAGAG | 140456 |
rs188178424 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15293802 | TAGAAAATAGCCATC[A/G]ACATTTTCTTAATCC | 140456 |
rs188266830 | snp | A/C | 0.00738971 | 0.0603345 | | | GRCh38.p7 | X:15280244 | GCATAATTCTACTCT[A/C]TGTTTCTGTGAGCTC | 140456 |
rs188280468 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15313529 | AAATAAAACTGGGAA[A/G]TTAACATGCACCATT | 140456 |
rs188394690 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306947 | CATGGCTGCCAGCTC[A/G]GCACCCTGACCAATG | 140456 |
rs188408229 | snp | C/T | 0.0204488 | 0.0990265 | | | GRCh38.p7 | X:15276355 | GTAGTCTTGTTCTGT[C/T]GCCCAGGCTGGAGTG | 140456 |
rs188418068 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15306669 | GATCACGCCATTGCA[C/T]TCCAGCTTGGGTGAC | 140456 |
rs188535460 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15297099 | GAGATCAAGACCATC[C/T]TGGCTAACACAGTGA | 140456 |
rs188673699 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15315373 | ACTAGTCATATGAAT[G/T]ATCTAGGAGGGATTT | 140456 |
rs188691407 | snp | A/G | 0.0121112 | 0.0768695 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281855 | GGCACCTGCCACCAC[A/G]CCTGGCTAACTTTTG | 140456 |
rs188706356 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | ASB11 | GRCh38.p7 | X:15286614 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 140456 |
rs188779336 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15290170 | CCATGCTTCCCCACT[C/G]CAGCTCCTCTTTACA | 140456 |
rs188781256 | snp | A/G | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316753 | GTGCTAGGATTACAG[A/G]TGTGAGCCACTGCAC | 140456 |
rs188814485 | snp | A/G | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15277108 | TCTATGTTAAATCAG[A/G]CAAAGGAATAAAAAA | 140456 |
rs188822092 | snp | C/T | 0.0323082 | 0.122924 | intron-variant | ASB11 | GRCh38.p7 | X:15301095 | AGCCTCCCAAGTAGC[C/T]GGGATTATAGGCGCC | 140456 |
rs188897006 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15301904 | ATAGGCAGCCTCTAA[A/G]ATAGCACCCAGTAAT | 140456 |
rs188910762 | snp | A/G | 0.190717 | 0.242869 | intron-variant | ASB11 | GRCh38.p7 | X:15295584 | AGGTCCCAGAGGGAA[A/G]AACATGATAAGCTCA | 140456 |
rs188931388 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299874 | ACCCTGAACCCCGAA[C/T]TCCTACTTACACGGC | 140456 |
rs188931891 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | ASB11 | GRCh38.p7 | X:15284018 | AGCACTTTGGGAGGC[C/T]AAGGTGGGCGGATCA | 140456 |
rs189200812 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15312871 | ATAATTTAGGAATTA[A/G]AGAGACTGAGGGGTT | 140456 |
rs189225030 | snp | A/C | | | | | GRCh38.p7 | X:15278894 | CCTTTGCTAATATTT[A/C]TATTCATGAACCTAT | 140456 |
rs189405930 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15285286 | GGTGGGATTACAGGC[A/G]GGTGCCACCAAACCC | 140456 |
rs189434081 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15305207 | CAGTGATGGAACAGA[C/T]TGTCATCTGATGGAA | 140456 |
rs189434634 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15313315 | GAGGCACGAGAATTG[C/T]TTGAACCCCAGAGGA | 140456 |
rs189660475 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314891 | GAATAAACTTTGTTT[G/T]GAGTGCTTTGCATGC | 140456 |
rs189682977 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15305344 | GGAAACTGTGCACCA[A/G]CCCAAACTGAGGGGA | 140456 |
rs189838351 | snp | A/G | 0.0026455 | 0.0362733 | | | GRCh38.p7 | X:15275647 | AAATGCTAACAATTG[A/G]TGAATTGAGGTGATG | 140456 |
rs189913638 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15314212 | GAAGAATGATTTATC[A/T]ATGAGAACACCAAAA | 140456 |
rs189950189 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15299245 | CCAGAGAACATGTGC[C/T]CAGGGTAGTCAGGGC | 140456 |
rs189954323 | snp | C/G/T | 0.00370173 | 0.0428621 | | | GRCh38.p7 | X:15280497 | TGAATAGAGCTACAA[C/G/T]AAACATGGAGGTGCA | 140456 |
rs189966120 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15307999 | CCTTCTCCAGCCCAC[C/T]CAGCAGCTGGAGACA | 140456 |
rs189969315 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15308870 | GGCCTGTTAGGAACC[A/G]GGCTGCACAGCAGGA | 140456 |
rs189973709 | snp | A/G | 0.0425 | 0.139441 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283004 | TACGTATATGTATGT[A/G]TATATATATACGTAT | 140456 |
rs190005184 | snp | A/C | 0.0276852 | 0.114351 | | | GRCh38.p7 | X:15276602 | GATTACAGGCGTGAG[A/C]CACTGCGCCCAGCCT | 140456 |
rs190165004 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15311446 | GTTTGTGGAGACAAC[C/T]AGCAAAACTAAATAA | 140456 |
rs190196486 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15294625 | ACCCTCCTGCCTCAG[C/T]CTGCCAAAGGGCAGG | 140456 |
rs190200569 | snp | A/C | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:15278067 | TGCCTTAGACCACCC[A/C]ACTTCCCTAACCCGT | 140456 |
rs190223881 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317275 | AATTTCTCCTAGCAT[A/G]CAGGCAAATTAGAAT | 140456 |
rs190228484 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15289845 | CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 140456 |
rs190258709 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15283798 | TACAGACAGCAGATC[C/G]TGATTTGCCCCTCTG | 140456 |
rs190500317 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297866 | CTGCATTAGTGATAG[A/C]AATGAAAGCAATGTT | 140456 |
rs190585218 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15303370 | ATCACAAAAAAATCT[C/T]GTAAGTTTTACGAAA | 140456 |
rs190720414 | snp | A/T | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15313972 | CAGGAGAATTGCTTC[A/T]ACCGGGACCTGGGAG | 140456 |
rs190738376 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15280397 | TTTTAAGGCTGAATA[A/G]TATTTCATTTTGTAT | 140456 |
rs190751665 | snp | A/C/G | 0.00634021 | 0.0559831 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281729 | TTGAGACGGAGTCTC[A/C/G]CTCTGTCACCCAGGC | 140456 |
rs190751771 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305783 | TGACTTTTATCTTAA[C/G]TTCAGGGGTACATGT | 140456 |
rs190866004 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15277437 | GGCACATAGTAGATG[C/T]CAAGTAAAAAATGTA | 140456 |
rs190873766 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | ASB11 | GRCh38.p7 | X:15309469 | TTATGGTGAGTTGTA[A/T]AATTATTTGATTATA | 140456 |
rs190882079 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15291714 | TCTGTCTCAAAAAAT[A/T]AAAAAAAAATTTAAA | 140456 |
rs190967675 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299582 | TGATGTTAAATTCTG[G/T]TCATCTTTTCCTGAG | 140456 |
rs190990156 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15285774 | TTTGGGAGGCTGAGG[C/G]GGGTGGATCACCTGA | 140456 |
rs191005294 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15287569 | TGACCTTGTGATCCA[C/T]CCGCCTCAGCCTCCC | 140456 |
rs191108660 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15286544 | GTGGTGCACGCCTGT[A/G]GTCCCAGCTACTCAG | 140456 |
rs191116401 | snp | C/T | 0.00528398 | 0.051128 | | | GRCh38.p7 | X:15275999 | GTTGTGGTTATTCAG[C/T]GATTCATCCCTCACC | 140456 |
rs191121716 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306214 | TCTTTGTTATTGTGA[C/T]TAGTGCTGTAATGAA | 140456 |
rs191193193 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15307087 | GGATTTAAGTGGCAA[C/T]TTGCAATTAAAAGAG | 140456 |
rs191207478 | snp | G/T | 0.0635374 | 0.166528 | | | GRCh38.p7 | X:15276521 | ACGGGGTTTCACCGT[G/T]TTAGCCAGGATGGTC | 140456 |
rs191224849 | snp | A/G | 0.017851 | 0.0927731 | intron-variant | ASB11 | GRCh38.p7 | X:15288890 | AACTTCATCTCAAAA[A/G]AAAAAAAGATATTTC | 140456 |
rs191231626 | snp | C/T | 0.0758246 | 0.17934 | | | GRCh38.p7 | X:15276385 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 140456 |
rs191242049 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15306680 | TGCACTCCAGCTTGG[A/G]TGACACAGTGACACT | 140456 |
rs191262452 | snp | A/C | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15302869 | TGTAACTTGTCCATG[A/C]TGCCCACCCACTGTG | 140456 |
rs191458377 | snp | A/C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15312397 | CAGACTATGAAATCC[A/C/G]CCCCCACCCGCCCAC | 140456 |
rs191474369 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15284963 | CCATGAGATAGAAAG[A/C]TACCTGGAGGACCAA | 140456 |
rs191514092 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15310470 | TTCAAGTGCTTTTTC[A/C]TTTCCCCCTTTGAAT | 140456 |
rs191535055 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15277632 | TTAATTTGATCAGGT[C/T]TGTCCGCCCTGCTTG | 140456 |
rs191536203 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15284060 | GATGGAGACCATCCT[G/T]GCTAACACGGTGAAA | 140456 |
rs191798849 | snp | G/T | 0.0333324 | 0.12472 | intron-variant | ASB11 | GRCh38.p7 | X:15284189 | CCCGGGAGGCGGAGC[G/T]TGCAGTGAGCCGAGA | 140456 |
rs191807345 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297217 | GAATGGCGTGAACCC[C/T]GGCAGAGCTTGCAGT | 140456 |
rs191809227 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15293418 | AGAGGAATTCCCCAC[A/G]CTGGTGAATAAGTGA | 140456 |
rs191817813 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15313354 | CACTGAGCTAAGATC[A/G]TGCCACTGAACTCCA | 140456 |
rs192088887 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15284214 | CCGAGATCGGGCCAC[A/T]GCACTCCAGCCTGGG | 140456 |
rs192092022 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15303032 | GAGAAGGAACAGTCA[A/G]TCTCTCTGGCTTTTG | 140456 |
rs192208429 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316964 | AAAATGTGGGCTATC[C/T]TTGATCATGGAAGAG | 140456 |
rs192223431 | snp | C/G | 0.00105904 | 0.0229869 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283045 | AAAATCAAAATTATA[C/G]CAGATTTATTCAAGG | 140456 |
rs192333407 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282662 | AATAACAGCATTTAA[C/T]ATCAGAAGCAATAAG | 140456 |
rs192340129 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316473 | TATGCATGTATGCAC[G/T]TATGTATGTATTTAG | 140456 |
rs192342969 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15300553 | ATAAAGAATGCCCCC[G/T]TACACATTTAACCAT | 140456 |
rs192523341 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15307297 | AAAAGAACATGTACC[A/G]TGTGATTTGGTTTCT | 140456 |
rs192647977 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15301101 | CCAAGTAGCTGGGAT[A/T]ATAGGCGCCCACCAC | 140456 |
rs192737035 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15304387 | CGAGGTTGGATTGAT[A/G]TTGGAGCAATTAGCA | 140456 |
rs192794717 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15304555 | CCAGGTCTGGGCCAG[A/G]TAAAATACAAGATGG | 140456 |
rs192865497 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15312902 | GAGGAGGATTTATTG[G/T]TTAGGTGTATTGGCC | 140456 |
rs192872642 | snp | A/G | 0.00528398 | 0.051128 | | | GRCh38.p7 | X:15279833 | AAAAAGAAAGCCAGT[A/G]AAATTAATTTTAATA | 140456 |
rs192948735 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284702 | GGAAAATCAGCTGAT[C/G]AGAGTCCAGAATATG | 140456 |
rs193061027 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15295792 | ATTCTTCTCTTTGTG[C/T]CCAACAAAACCTCCT | 140456 |
rs193112874 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15300008 | TCTGTCTATTTTCAT[A/G]TCCTGAATATGACAT | 140456 |
rs193116566 | snp | A/G | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15276553 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCGT | 140456 |
rs193209182 | snp | A/T | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15278751 | TCTTTGATCGTTCCA[A/T]GGCTAATGATGGCTC | 140456 |
rs193268504 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282278 | TACTGAACCATGACA[A/G]TAATACTTACAATAA | 140456 |
rs193271798 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315925 | TTTATGTTAGAAAGC[A/C]GGGTTGGAAAGATAG | 140456 |
rs199507047 | in-del | -/A | 0.0394543 | 0.134798 | intron-variant | ASB11 | GRCh38.p7 | X:15305585 | AAACATTTTAACAAG[-/A]AAAAAAAAAGATTAG | 140456 |
rs199531193 | in-del | -/TTTC | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281677 | TTTTTTTTGTTTGTT[-/TTTC]TTTCTTTCTTTCTTT | 140456 |
rs199538988 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15285140 | TGGTATTTAATCTTT[C/T]TTTTTTTTTTTTTTT | 140456 |
rs199598614 | snp | C/T | 0.000113938 | 0.00754692 | missense | ASB11 | GRCh38.p7 | X:15283528 | ATAGGAGGAATCGTT[C/T]GAGTGGCTCTGGCAG | 140456 |
rs199601166 | snp | C/T | 7.47906e-05 | 0.00611471 | intron-variant | ASB11 | GRCh38.p7 | X:15287840 | AGGAAGGGGAGAGAA[C/T]GTGCTTATGGAAGAG | 140456 |
rs199612828 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15284037 | GTGGGCGGATCACGA[G/T]GTCAGGAGATGGAGA | 140456 |
rs199617954 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15312841 | TTTTAATACACCTAA[A/C]TATATTGTTATGGGA | 140456 |
rs199772709 | in-del | -/TTATC | 0.0460406 | 0.14457 | intron-variant | ASB11 | GRCh38.p7 | X:15305774 | TATGTTTTTTGACTT[-/TTATC]TTAAGTTCAGGGGTA | 140456 |
rs199834678 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15284193 | GGAGGCGGAGCTTGC[A/G]GTGAGCCGAGATCGG | 140456 |
rs199945565 | snp | C/G | 6.83776e-05 | 0.00584672 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283498 | ATCTTCCCAGGAACA[C/G]TTAGGACTATTGGTA | 140456 |
rs200099511 | in-del | -/TA | 0.0121112 | 0.0768695 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283016 | GTATATATATATACG[-/TA]TATATATATACAAAA | 140456 |
rs200164931 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15289007 | TAGCCTGTAGCAAAT[A/G]TCTGTTTTTACCGTC | 140456 |
rs200347568 | in-del | -/AG | | | intron-variant | ASB11 | GRCh38.p7 | X:15301515 | CATGCACACACAGAC[-/AG]AGAGAGAGAGACAGA | 140456 |
rs200380702 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15313498 | ACACACACACATATA[C/T]ATATATATATGAAAG | 140456 |
rs200484757 | snp | A/C | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316407 | AGCAAGATTCTGTCT[A/C]AAAAAAAAAAAAAAA | 140456 |
rs200505753 | in-del | -/A | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282197 | TAGAAAAATTGGGGG[-/A]AAAAAAAACATGTGT | 140456 |
rs200543900 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15291727 | ATAAAAAAAAAATTT[A/T]AAAAAATTAAAAAAA | 140456 |
rs200579705 | in-del | -/CA | | | intron-variant | ASB11 | GRCh38.p7 | X:15313477 | ACACACACACACACA[-/CA]TATACATATATATAT | 140456 |
rs200637615 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15306039 | ATTTGGTTTTCTGTT[C/T]CTGTTAGTTTTCTAA | 140456 |
rs200681166 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15306016 | ACTTATAAGTGAGAA[A/C]ATGTGGCATTTGGTT | 140456 |
rs200705921 | snp | A/G | 0.000705167 | 0.018764 | intron-variant | ASB11 | GRCh38.p7 | X:15288111 | TTCAACACTAAATGT[A/G]ATGTAAAGCACAATG | 140456 |
rs200827560 | in-del | -/A | 0.0358881 | 0.129059 | intron-variant | ASB11 | GRCh38.p7 | X:15297304 | AAAACAAAACAAAAC[-/A]AAAACAAAAAAAAAA | 140456 |
rs200869756 | in-del | -/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15297309 | CAAAACAAAACAAAA[-/C]AAAAAAAAAACATGG | 140456 |
rs200893386 | in-del | -/AAC | | | intron-variant | ASB11 | GRCh38.p7 | X:15286025 | AATAATAATAATAAT[-/AAC]AATAATAATAATCTA | 140456 |
rs200897958 | in-del | -/TG | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282955 | AAATATATGAGTGCA[-/TG]TGTGTGTGTGTATAT | 140456 |
rs200912767 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15313500 | ACACACACATATACA[C/T]ATATATATGAAAGAA | 140456 |
rs201012334 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15297122 | CACAGTGAAACTCTG[C/T]CTCTACTAAAAATAC | 140456 |
rs201059601 | in-del | -/T | 0.0348667 | 0.127349 | intron-variant | ASB11 | GRCh38.p7 | X:15287336 | GGTTTTCTGGTTTTC[-/T]TTTTTTTTGAGACGG | 140456 |
rs201079816 | snp | C/T | 2.28027e-05 | 0.00337651 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283482 | CTGTGTCATTCCAAG[C/T]ATCTTCCCAGGAACA | 140456 |
rs201132091 | in-del | -/T | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281661 | TGTACCTGATAATTC[-/T]TTTTTTTTGTTTGTT | 140456 |
rs201156950 | snp | A/G | 4.71832e-05 | 0.00485689 | synonymous-codon | ASB11 | GRCh38.p7 | X:15287909 | GAGTGCCTGCTCCAC[A/G]CTGCTTTTTGGAGCC | 140456 |
rs201248205 | in-del | -/A | 0.0630423 | 0.165972 | intron-variant | ASB11 | GRCh38.p7 | X:15313040 | CAGTGGTATCAAAAG[-/A]AAAAACACAGAACCA | 140456 |
rs201290024 | in-del | -/T | 0.0126344 | 0.0784702 | intron-variant | ASB11 | GRCh38.p7 | X:15304477 | GTGCGTATATACGTA[-/T]TTTTTTTTTAGCATG | 140456 |
rs201374291 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15288732 | CTACTAAAAATACAA[A/T]AAATTAGCCGGGTGT | 140456 |
rs201380011 | snp | A/G | 6.83706e-05 | 0.00584642 | stop-lost | ASB11 | GRCh38.p7 | X:15283507 | GGAACACTTAGGACT[A/G]TTGGTATAGGAGGAA | 140456 |
rs201426380 | snp | C/T | 2.27889e-05 | 0.00337549 | missense | ASB11 | GRCh38.p7 | X:15283524 | TGGTATAGGAGGAAT[C/T]GTTCGAGTGGCTCTG | 140456 |
rs201610277 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15306023 | AGTGAGAACATGTGG[C/T]ATTTGGTTTTCTGTT | 140456 |
rs201650061 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15306051 | GTTCCTGTTAGTTTT[C/T]TAAGGATAATGGCCT | 140456 |
rs201659261 | in-del | -/T | 0.110818 | 0.207674 | intron-variant | ASB11 | GRCh38.p7 | X:15314330 | TATCAGAAGCATTAC[-/T]TTTTTTTTTTTTTTT | 140456 |
rs201791187 | in-del | -/T | 0.0465453 | 0.14528 | intron-variant | ASB11 | GRCh38.p7 | X:15301230 | GGCCTCCTAAAGTGC[-/T]AGGATTACAGGCGTG | 140456 |
rs201885038 | in-del | -/TA | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282978 | GTGTATATATATACG[-/TA]TATATATATATACGT | 140456 |
rs201981973 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15313494 | ACACACACACACACA[C/T]ATACATATATATATG | 140456 |
rs202017413 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15300391 | TCACATTAGCTTAAT[G/T]TTTTACTCATATCGG | 140456 |
rs202091307 | snp | A/T | 2.3165e-05 | 0.00340323 | missense | ASB11 | GRCh38.p7 | X:15293211 | GAGGCCAGGTGCACC[A/T]CCAACTGGGCCTTGG | 140456 |
rs202179448 | snp | C/T | 2.27889e-05 | 0.00337549 | missense | ASB11 | GRCh38.p7 | X:15283575 | GCTTGATGACATGCT[C/T]GACCGAGACACTTCC | 140456 |
rs367547271 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15284053 | GTCAGGAGATGGAGA[C/T]CATCCTGGCTAACAC | 140456 |
rs367631030 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282800 | TAACTTTATATATGT[A/G]TATATATATAAAGTC | 140456 |
rs367968494 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15307668 | CCCTGCTATAAAGTA[C/T]ACAAGGAAGGGAAAC | 140456 |
rs368002578 | snp | C/T | 0.000114403 | 0.00756231 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15314423 | TCTCTTTCCATGGTC[C/T]GGACCTTCTGATACG | 140456 |
rs368172465 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15302643 | CTGGATAGGGTGAGC[C/T]ACACCTCTGCTACAG | 140456 |
rs368211805 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15291504 | TGAGGTCAGGAGTCT[C/G]AGACCAGCCTGGCCA | 140456 |
rs368389838 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15309655 | TGGTGTGAAATAAAC[C/G]AATTGTACCACCCTA | 140456 |
rs368403151 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15313095 | GTTACTGCCTACATT[C/T]TTATAGAAAGACTTA | 140456 |
rs368512399 | snp | C/T | 0.000114032 | 0.00755002 | missense | ASB11 | GRCh38.p7 | X:15289570 | CATATAGGGGAGTTC[C/T]GAGCTGAGGCACCTC | 140456 |
rs368515454 | snp | A/C | 0.00158814 | 0.0281345 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281738 | AGTCTCGCTCTGTCA[A/C]CCAGGCTGGAGTGCA | 140456 |
rs368531308 | multinucleotide-polymorphism | CC/GG | | | intron-variant | ASB11 | GRCh38.p7 | X:15284207 | CAGTGAGCCGAGATC[CC/GG]GCCACTGCACTCCAG | 140456 |
rs368605491 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297031 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 140456 |
rs368639487 | snp | C/T | 9.20111e-05 | 0.00678212 | synonymous-codon | ASB11 | GRCh38.p7 | X:15287936 | AGCCGCCAGATCAAG[C/T]GCACTTTTGCCCTGA | 140456 |
rs368798540 | snp | C/T | 2.31744e-05 | 0.00340392 | intron-variant | ASB11 | GRCh38.p7 | X:15302826 | AAACACAAATCAAGC[C/T]CAAAGTCAAGGCCTG | 140456 |
rs368958292 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15295496 | TAAGATGACTCTCAG[A/G]TTTGCAGCTTGGGAA | 140456 |
rs369084992 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15289796 | TGGGAGGCTGAGACC[A/G]GCGGATTCCCTGAGG | 140456 |
rs369086088 | snp | C/G | 2.41797e-05 | 0.00347696 | intron-variant | ASB11 | GRCh38.p7 | X:15293160 | ACATGCATTGTGGTG[C/G]CTCATTTACCTCTCT | 140456 |
rs369128675 | snp | A/G | 6.95467e-05 | 0.00589648 | upstream-variant-2KB, synonymous-codon | ASB11 | GRCh38.p7 | X:15315486 | TCTATTTCCTTTGAC[A/G]ATATAGAAATGGGTT | 140456 |
rs369164286 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15311741 | AATTCTGAAAACCAA[G/T]CTTTACCCCAAATTT | 140456 |
rs369166617 | snp | A/G | | | | | GRCh38.p7 | X:15276703 | AGATGGTAAATACAT[A/G]TATGTCTACATAGAC | 140456 |
rs369200134 | in-del | -/A | 0.285075 | 0.247527 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316407 | GCAAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 140456 |
rs369335076 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15286692 | AAAAAAAAAGTGCAC[A/G]CTCTGGGGTCAGATG | 140456 |
rs369472683 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15309563 | AAAACCATCCCCCCA[C/T]ACCCTGGTCCATGGA | 140456 |
rs369531997 | snp | A/G | | | | | GRCh38.p7 | X:15276434 | CCATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT | 140456 |
rs369546543 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15305953 | CCAATAGGCCCCAGT[A/G]TATGTTGTTCCCCTC | 140456 |
rs369572478 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15290996 | TTGGAAAATACAGGG[C/T]ATTTAATACATATTT | 140456 |
rs369669512 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15297448 | CTAAATGATGGAATA[C/T]GGACATGGATAGAAC | 140456 |
rs369699016 | snp | A/G | 2.41996e-05 | 0.00347839 | intron-variant | ASB11 | GRCh38.p7 | X:15293349 | AAGAGAGACCCAAAG[A/G]ATTTGTTATTTCATT | 140456 |
rs369845737 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15283991 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 140456 |
rs369934462 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15305592 | TTTAACAAGAAAAAA[A/T]AAGATTAGATAGATA | 140456 |
rs369954787 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15295990 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 140456 |
rs370004685 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15310713 | GACCCAACAGCCGGG[C/T]GCGGTGGCTTATGCC | 140456 |
rs370005474 | snp | A/G | 0.000191981 | 0.0097956 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315652 | CTGTAAAATTTCACT[A/G]AGTTATAATTGGTAT | 140456 |
rs370120817 | snp | C/T | 6.91005e-05 | 0.00587754 | missense | ASB11 | GRCh38.p7 | X:15293265 | ACACATGCAGCACTG[C/T]CGCTGCAGCAAGCAT | 140456 |
rs370192036 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15299456 | ATGTCTGTCTGGGTT[A/T]CAATAAGGGGTTGTG | 140456 |
rs370303393 | snp | C/T | 2.45628e-05 | 0.0035044 | splice-donor-variant | ASB11 | GRCh38.p7 | X:15297573 | CAGGGGCAGTACTCA[C/T]GTGTGCACCATTTTC | 140456 |
rs370379622 | snp | A/C | 2.28514e-05 | 0.00338011 | missense | ASB11 | GRCh38.p7 | X:15302775 | GCCCCTGAGCTGCAG[A/C]TTCATGAAGTGGGGA | 140456 |
rs370406921 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281854 | AGGCACCTGCCACCA[C/T]GCCTGGCTAACTTTT | 140456 |
rs370496546 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15305595 | AACAAGAAAAAAAAA[A/G]ATTAGATAGATAGAT | 140456 |
rs370524937 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15291984 | AGGTTGCAATGAGCA[A/G]AAATCATGCCACTGC | 140456 |
rs370659065 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15313219 | GCCTGGCCAACATAG[C/G]GAAACCCCATCTCTA | 140456 |
rs370909136 | snp | A/G | | | | | GRCh38.p7 | X:15275343 | TGCCTCACTCACCTA[A/G]TCCTGATTCTAGCCC | 140456 |
rs371206927 | snp | C/T | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316472 | GTATGCATGTATGCA[C/T]GTATGTATGTATTTA | 140456 |
rs371299066 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15284173 | AGGAGAATGGCGTGA[A/G]CCCGGGAGGCGGAGC | 140456 |
rs371550216 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15294988 | TGGGCTGAACAATTG[C/T]CTCTCCTTGAGTAGG | 140456 |
rs371623135 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15284028 | GAGGCCAAGGTGGGC[A/G]GATCACGAGGTCAGG | 140456 |
rs371751531 | snp | A/G/T | 0.000253965 | 0.011266 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315499 | ACGATATAGAAATGG[A/G/T]TTAGGAGAGCCAAAA | 140456 |
rs371900911 | snp | A/G | 9.47362e-05 | 0.0068818 | utr-variant-5-prime, intron-variant | ASB11 | GRCh38.p7 | X:15314534 | TTAGATAAGACTGCT[A/G]TTGTCTAGTGTCTTC | 140456 |
rs371916534 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15295519 | CTTGGGAAACCAAGA[A/G]GATGTTTCTTTCACC | 140456 |
rs372034466 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314712 | ATGAATAAATACTCC[G/T]CTATTAAGTGACAAT | 140456 |
rs372168670 | snp | C/G | 0.000377928 | 0.0137412 | missense | ASB11 | GRCh38.p7 | X:15287952 | GCACTTTTGCCCTGA[C/G]CATTTCTACGCTTCA | 140456 |
rs372305999 | snp | C/T | 0.0266548 | 0.112325 | intron-variant | ASB11 | GRCh38.p7 | X:15284112 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGTGCC | 140456 |
rs372322666 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15314117 | AAAGACAGAAATAAT[A/G]CGCAGGTGCAACAGG | 140456 |
rs372368436 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15297249 | AGCGGAGATTGTGCC[A/G]CTGCACTCCAGCCTG | 140456 |
rs372379424 | snp | A/G | 0.000387977 | 0.0139226 | missense | ASB11 | GRCh38.p7 | X:15289593 | GGCACCTCATGGTCA[A/G]TGTTAACATTATTTG | 140456 |
rs372476532 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15309836 | AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 140456 |
rs372594541 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282477 | AAATATTGACCCAGC[A/G]TTGAGCCCACTTTGG | 140456 |
rs372622627 | in-del | -/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15291447 | TAATAAAGACTTTTT[-/T]GTAATACCAGCACTT | 140456 |
rs372714933 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15311939 | GACAGTATGCACATT[A/G]TATGATCTTTCTAAC | 140456 |
rs372821055 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15283956 | ATTGAATGTGCCAAT[G/T]AAAGTGATACACGGG | 140456 |
rs372823923 | in-del | -/A | | | | | GRCh38.p7 | X:15280655 | TTTCTCCAAAAAAAA[-/A]GACATACAAATGGCC | 140456 |
rs372905292 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15306576 | GGCACGGTGGTAGGC[A/G]CCTGTAATCCCAGCT | 140456 |
rs373371394 | snp | C/G | 0.00633741 | 0.0559334 | intron-variant | ASB11 | GRCh38.p7 | X:15290615 | GCTTTGTTCAGGAGA[C/G]AGTGCTTCTGAGGTA | 140456 |
rs373380884 | snp | A/T | | | | | GRCh38.p7 | X:15279067 | GATTTGTGAAAATTG[A/T]CTTTCCTAAGGTTTG | 140456 |
rs373391834 | snp | A/G | | | | | GRCh38.p7 | X:15276959 | CTAGAAATAATTTAA[A/G]TATCTAACAATATGG | 140456 |
rs373533421 | snp | C/T | 4.60861e-05 | 0.0048001 | missense | ASB11 | GRCh38.p7 | X:15293266 | CACATGCAGCACTGC[C/T]GCTGCAGCAAGCATT | 140456 |
rs373538907 | snp | A/G | 7.38925e-05 | 0.00607789 | intron-variant | ASB11 | GRCh38.p7 | X:15297562 | ACCCAAGTGGGCAGG[A/G]GCAGTACTCACGTGT | 140456 |
rs373647947 | snp | G/T | 0.00121898 | 0.0246577 | intron-variant | ASB11 | GRCh38.p7 | X:15287875 | GGATACCCAGCCCTT[G/T]GTTACCTTCACGGAG | 140456 |
rs373650075 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15298518 | TCTTAGAGGAAATGG[A/G]GCACCTATGAAGTCT | 140456 |
rs373751514 | snp | C/T | 0.000189982 | 0.00974449 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15297672 | TTGTCACAAGGTTCA[C/T]ATTGACACCCTATAA | 140456 |
rs373961049 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15302097 | GCACTCTCTCTGAGA[C/G]AAGCCAGCTGCCATC | 140456 |
rs373976469 | snp | A/G | 0.0266548 | 0.112325 | intron-variant | ASB11 | GRCh38.p7 | X:15284129 | TGGTGGCGGGTGCCT[A/G]TAGTCCCAGCTACTC | 140456 |
rs374004390 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15291253 | GTTTATTATGAGCAT[A/G]TATATGTTTTATAGG | 140456 |
rs374022879 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15305593 | TTAACAAGAAAAAAA[A/T]AGATTAGATAGATAG | 140456 |
rs374065486 | snp | C/G | 4.56069e-05 | 0.00477508 | missense | ASB11 | GRCh38.p7 | X:15283618 | GGCAGAGCTGGGAAA[C/G]AGCAGGTGGGCCTGA | 140456 |
rs374398541 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15286663 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 140456 |
rs374424366 | in-del | -/G | 0.00187734 | 0.0305801 | intron-variant | ASB11 | GRCh38.p7 | X:15314347 | TTTTTTTTTTTTTTT[-/G]TAACTAGTCAAAGTA | 140456 |
rs374507690 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15296545 | TATTCTGATATCTGT[A/C]TTATATATTGCACCT | 140456 |
rs374545467 | in-del | -/TG | | | intron-variant | ASB11 | GRCh38.p7 | X:15305337 | ATAAGGAGGAAACTG[-/TG]CACCAACCCAAACTG | 140456 |
rs374550985 | snp | C/T | 0.000116129 | 0.00761913 | synonymous-codon | ASB11 | GRCh38.p7 | X:15293207 | GGGCGAGGCCAGGTG[C/T]ACCTCCAACTGGGCC | 140456 |
rs374605946 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15296167 | GGCAGGGGAATCGTT[A/C]GAATCTAGGAAGTGG | 140456 |
rs374678173 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15290088 | AGCATAAAAACATTT[C/T]TGTGTTTGTTTTTGG | 140456 |
rs374697501 | snp | A/G | 0.000189982 | 0.00974449 | intron-variant | ASB11 | GRCh38.p7 | X:15302824 | TGAAACACAAATCAA[A/G]CTCAAAGTCAAGGCC | 140456 |
rs374822961 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15292386 | TTCTGATCTCAGTAT[A/G]AGAGAACAACTCCCT | 140456 |
rs374860221 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282739 | CTTATCAACCAGGAC[C/T]GCAGTAACTGGAAGC | 140456 |
rs374883318 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15305596 | ACAAGAAAAAAAAAG[A/G]TTAGATAGATAGATA | 140456 |
rs375370513 | snp | A/G | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315659 | ATTTCACTGAGTTAT[A/G]ATTGGTATCATATGA | 140456 |
rs375554656 | snp | G/T | 0.00015707 | 0.00886061 | intron-variant | ASB11 | GRCh38.p7 | X:15314335 | GAAGCATTACTTTTT[G/T]TTTTTTTTTTTGTAA | 140456 |
rs375575418 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15299522 | GGTAGCAGGCTTCAG[-/A]GAGAATAGATTGTAA | 140456 |
rs375696907 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15284106 | AAATACAAAAAATTA[G/T]CCGGGTGTGGTGGCG | 140456 |
rs375735888 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15304687 | GTTCGAGACCAGCCT[A/G]GCCAGCATGGTGAAA | 140456 |
rs375790534 | snp | C/T | 2.32062e-05 | 0.00340625 | intron-variant | ASB11 | GRCh38.p7 | X:15302721 | ATCAAGTCTTCAGTT[C/T]ACTTACTTGTGCAAT | 140456 |
rs375889841 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15285235 | CAACCTCTGCCTCCC[A/G]GGTTTAGGCAGTTCT | 140456 |
rs375899924 | snp | A/C | 2.35638e-05 | 0.0034324 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315564 | AGCAAACATTGTAAT[A/C]AAAATGTTTTTAAAG | 140456 |
rs375923007 | snp | A/G | 2.34957e-05 | 0.00342743 | intron-variant | ASB11 | GRCh38.p7 | X:15283676 | ATAGTGGTGGGAGGT[A/G]GGGTGGAAGGGGGAA | 140456 |
rs376007321 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15313077 | AAATACTGGTCCAGG[C/T]ATGTTACTGCCTACA | 140456 |
rs376014454 | snp | A/G | 4.5621e-05 | 0.00477581 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283457 | TACTCTAGGTACAGC[A/G]GACAACAATCTGTGT | 140456 |
rs376027677 | snp | A/G | 0.000189982 | 0.00974449 | intron-variant | ASB11 | GRCh38.p7 | X:15297566 | AAGTGGGCAGGGGCA[A/G]TACTCACGTGTGCAC | 140456 |
rs376028460 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15299590 | AATTCTGGTCATCTT[C/T]TCCTGAGTTCCAAAA | 140456 |
rs376376953 | snp | C/T | 0.000189982 | 0.00974449 | missense | ASB11 | GRCh38.p7 | X:15293230 | ACTGGGCCTTGGCTC[C/T]GAACTCCAGCAGCAC | 140456 |
rs376596703 | snp | C/T | 0.0276852 | 0.114351 | intron-variant | ASB11 | GRCh38.p7 | X:15284124 | GGGTGTGGTGGCGGG[C/T]GCCTATAGTCCCAGC | 140456 |
rs376664949 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15291752 | AAAAAAAAAGACTTA[C/T]ATGGCTGAGCACGGT | 140456 |
rs376687588 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15284149 | CCCAGCTACTCGGGA[G/T]GCTGAGGCAGGAGAA | 140456 |
rs376817491 | snp | A/C | 2.48327e-05 | 0.0035236 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15315406 | TTTAAATATTAGGAA[A/C]AAATTCATGTACTTT | 140456 |
rs376844871 | snp | C/T | | | | | GRCh38.p7 | X:15279070 | TTGTGAAAATTGACT[C/T]TCCTAAGGTTTGCAA | 140456 |
rs376869808 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15308803 | CTTGGGTTGCTCTGA[A/C]ATCCACCTCCTCTTT | 140456 |
rs376929958 | snp | C/T | 2.32288e-05 | 0.00340791 | intron-variant | ASB11 | GRCh38.p7 | X:15289658 | TGGAACACAAGATAC[C/T]CTCACTCAAGTAAGG | 140456 |
rs377229925 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15312354 | ATGTAATAGTTTAAG[C/T]CACAAAGACATATAA | 140456 |
rs377291338 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15305925 | TCGTCTCACTCCTCC[C/T]ACCCTCCACCCTCCA | 140456 |
rs377462580 | snp | C/T | 0.00011701 | 0.00764795 | missense | ASB11 | GRCh38.p7 | X:15293299 | AGAGGGGTGTGGCTC[C/T]GTGAACTGTCACTCC | 140456 |
rs377554724 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15290714 | TACTAATTAATTTAG[A/C]CAACCTATTTTTTGT | 140456 |
rs377600976 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | ASB11 | GRCh38.p7 | X:15285330 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATCTT | 140456 |
rs377681865 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15305594 | TAACAAGAAAAAAAA[A/T]GATTAGATAGATAGA | 140456 |
rs377706601 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15305590 | ATTTTAACAAGAAAA[A/G]AAAAGATTAGATAGA | 140456 |
rs377707759 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15295190 | TGGGACTACAGGCGC[A/G]TGCCACCATGCCTAG | 140456 |
rs386824058 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ASB11 | GRCh38.p7 | X:15284023 | TTTGGGAGGCCAAGG[CA/TG]GGCGGATCACGAGGT | 140456 |
rs386824059 | multinucleotide-polymorphism | CCCGTGTCC/TCCATCTCT | | | intron-variant | ASB11 | GRCh38.p7 | X:15284077 | CTAACACGGTGAAAC[CCCGTGTCC/TCCATCTCT]ACTAAAAATACAAAA | 140456 |
rs386824060 | multinucleotide-polymorphism | ATC/GTG | | | intron-variant | ASB11 | GRCh38.p7 | X:15284080 | ACACGGTGAAACCCC[ATC/GTG]TCCACTAAAAATACA | 140456 |
rs386824061 | multinucleotide-polymorphism | AT/GC | | | intron-variant | ASB11 | GRCh38.p7 | X:15284119 | TAGCCGGGTGTGGTG[AT/GC]GGGTGCCTATAGTCC | 140456 |
rs386824062 | multinucleotide-polymorphism | CTA/TTG | | | intron-variant | ASB11 | GRCh38.p7 | X:15284127 | TGTGGTGGCGGGTGC[CTA/TTG]TAGTCCCAGCTACTC | 140456 |
rs386824063 | multinucleotide-polymorphism | ATAAC/GTTAT | | | intron-variant | ASB11 | GRCh38.p7 | X:15298336 | AGGAAGCAACAGGAA[ATAAC/GTTAT]TTCCTGTTGCTTCCT | 140456 |
rs386824064 | in-del | AA/TAG | | | intron-variant | ASB11 | GRCh38.p7 | X:15301230 | GGCCTCCTAAAGTGC[AA/TAG]GATTACAGGCGTGAG | 140456 |
rs397965630 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15296279 | TGGAAAAAAAAAAAA[-/A]CAAAAAAAGAAAATG | 140456 |
rs527238683 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15304986 | GTCCTCACTGATATA[A/T]ATGAATATATAAAGA | 140456 |
rs530064632 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15287274 | TGCTCAATCATACGC[G/T]TATGCCAGGACAGAA | 140456 |
rs530359592 | snp | A/G | 0.017851 | 0.0927731 | intron-variant | ASB11 | GRCh38.p7 | X:15295155 | TCAAGAGATTCTGCT[A/G]CCTTAGGCTCCCAAG | 140456 |
rs530872024 | in-del | -/AAAG | | | intron-variant | ASB11 | GRCh38.p7 | X:15284263 | CTCAAAAAAAAAAAA[-/AAAG]AAAAAAAGAAAGAAA | 140456 |
rs531483290 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15312044 | ACTATATTTTCTTTC[C/T]TGATGACCAAGTCAC | 140456 |
rs532500941 | snp | A/G | | | | | GRCh38.p7 | X:15275201 | CAATAATGCAGGGAC[A/G]TAAACAACAAGAGCC | 140456 |
rs532564335 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283201 | TGTTGACTTTTAGGT[A/G]CAAGAAGATCCCGAA | 140456 |
rs532675354 | snp | C/G | 0.000172931 | 0.00929708 | intron-variant | ASB11 | GRCh38.p7 | X:15287861 | TATGGAAGAGGAATG[C/G]ATACCCAGCCCTTGG | 140456 |
rs534266100 | snp | C/T | | | | | GRCh38.p7 | X:15278117 | CTTTGGGAAGGTGGA[C/T]TTGAGCACTGTTCTC | 140456 |
rs534296848 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15297118 | CTAACACAGTGAAAC[A/T]CTGTCTCTACTAAAA | 140456 |
rs534651361 | snp | G/T | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281545 | TCTTAATTCAGCCTA[G/T]CCACAATTCCTGTGC | 140456 |
rs536473916 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15310095 | CAAAGGACCTTCAAG[C/G]GTTTTCACACAGAAC | 140456 |
rs538804941 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15284034 | AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATGG | 140456 |
rs538929775 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | ASB11 | GRCh38.p7 | X:15298731 | ATGAGGTATAGATGA[C/T]GGAGTGCAGACAAGT | 140456 |
rs540193874 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314623 | AAATTGAAATGGATA[C/T]TAGATAAAGAATGAT | 140456 |
rs540394082 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15286600 | AACCCGGGAGGCAGA[A/G]GTTGCAGTGAGCCGA | 140456 |
rs540644152 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15285590 | AACTTCTATAAACTA[C/T]AGTCTCTGCTAACAG | 140456 |
rs542026463 | in-del | -/TA | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282979 | GTGTATATATATACG[-/TA]TATATATATACGTAT | 140456 |
rs542742803 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15284191 | CGGGAGGCGGAGCTT[A/G]CAGTGAGCCGAGATC | 140456 |
rs543524602 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317232 | TGGCCTAATAAATCT[C/T]AACAAATGATTTATG | 140456 |
rs546312941 | in-del | -/A | 0.0245906 | 0.108123 | intron-variant | ASB11 | GRCh38.p7 | X:15294350 | CCTTGCTTTGGACAC[-/A]AAAAAAAGACTTGTT | 140456 |
rs548791768 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15295441 | TAGAAAGTAAAATTA[A/G]CAGGAGTTTTTAATT | 140456 |
rs549569513 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15312105 | AAAGCTTGAAAAATC[A/G]TACAATACATCTCTC | 140456 |
rs550716454 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15288885 | AGCGAAACTTCATCT[C/T]AAAAAAAAAAAAGAT | 140456 |
rs553233637 | in-del | -/T | 0.0173352 | 0.0914717 | | | GRCh38.p7 | X:15276493 | GGCTAATTTTTTGTA[-/T]TTTTTAGTAGAGACG | 140456 |
rs553285599 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282375 | GGTGACAGAAGGAGA[A/G]AGAAATGAGAAGAAG | 140456 |
rs554601702 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15286410 | AGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG | 140456 |
rs554736908 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15312071 | TCACAGTACTAAACA[C/T]AGCTTAATACAAATT | 140456 |
rs557330668 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15299757 | TTATTTTTGATTTAT[A/G]AAAGGAATTAGGTCC | 140456 |
rs558769149 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15286619 | GCAGTGAGCCGAGAT[A/C]GCACCACTGCACTCC | 140456 |
rs560610195 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15288204 | TTTGAAAATATGCAA[C/T]TCAAGCCTAGAACCT | 140456 |
rs561464890 | snp | A/C/G | 0.0110715 | 0.0736511 | intron-variant | ASB11 | GRCh38.p7 | X:15284207 | CAGTGAGCCGAGATC[A/C/G]GGCCACTGCACTCCA | 140456 |
rs562118511 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15304557 | AGGTCTGGGCCAGGT[A/G]AAATACAAGATGGGC | 140456 |
rs562741660 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15291537 | ATGATGAAACCCTGT[C/T]TTTACTAAAAAATAC | 140456 |
rs563912588 | in-del | -/CA | 0.00581083 | 0.0535878 | intron-variant | ASB11 | GRCh38.p7 | X:15284076 | CTAACACGGTGAAAC[-/CA]CCCGTGTCCACTAAA | 140456 |
rs564346398 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15294767 | TTTATATTGCTAGGG[G/T]TTTCTATATTTTTAC | 140456 |
rs564940610 | snp | A/G | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316339 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 140456 |
rs565203154 | snp | C/T | 0.0256233 | 0.11025 | intron-variant | ASB11 | GRCh38.p7 | X:15287399 | TGGTGTGATCTCTGC[C/T]CATCGCAACCTCCGC | 140456 |
rs565670504 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15313414 | AAAACAAACAAAAAA[A/T]CAGAAAGTCTTATTT | 140456 |
rs567142562 | snp | A/C | 0.00317376 | 0.039709 | | | GRCh38.p7 | X:15278323 | AGGCCTTAAAAGGAA[A/C]TTAAAGATTACCTCT | 140456 |
rs567385401 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15295765 | ATTGACAAAGACAAG[A/G]AAACATGTCTTATTC | 140456 |
rs568248084 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15312670 | TGGGCTGGGACTTTT[A/G]TAAGTCAATTAGCTA | 140456 |
rs569337742 | snp | C/G | | | | | GRCh38.p7 | X:15275914 | TCCATGCAAGTGCCG[C/G]CCCTGGCAGTGATAA | 140456 |
rs569705470 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15314300 | AACTTTTCAGATCAT[A/G]CTTAACTTGAAACTT | 140456 |
rs571518526 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15298570 | AGCTAATAGATTAGC[C/T]TTTTTAGAAGCTTAC | 140456 |
rs572066167 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15302174 | TTTCCCAACAACCAC[A/G]TGAGTGAGTTTGAAA | 140456 |
rs572974986 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15286574 | GGAGGCTGAGGCAGA[A/G]AAATCGCTTGAACCC | 140456 |
rs573133485 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15284565 | AGGATTCCAGCTCAA[C/T]AGAGATCTGCAAGAA | 140456 |
rs573303390 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | ASB11 | GRCh38.p7 | X:15313638 | AGATTGAACAAGTAA[A/G]GATATTTGCACTACA | 140456 |
rs574200342 | snp | A/G | | | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314740 | AATCCCAGGAGTGAC[A/G]GGGATATCTGACTCA | 140456 |
rs575090648 | in-del | -/TTTT/TTTTT | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281696 | TTCTTTCTTTCTTTC[-/TTTT/TTTTT]TTTTTTTTTTTTTTG | 140456 |
rs575270074 | snp | A/G | | | | | GRCh38.p7 | X:15279985 | ATATTTTAATACCTA[A/G]AAGTAATCAAATCAG | 140456 |
rs575328540 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15300010 | TGTCTATTTTCATGT[C/T]CTGAATATGACATCA | 140456 |
rs575555103 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15284177 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 140456 |
rs576873872 | snp | C/T | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316623 | GGGATTACAGGCATG[C/T]GTCACCACGCCTGGA | 140456 |
rs577103728 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15292393 | CTCAGTATAAGAGAA[C/T]AACTCCCTCACTTGC | 140456 |
rs577239011 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15286950 | CAAATAATCAATATA[A/G]GCTCCGAAAATATTT | 140456 |
rs578016685 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283361 | TTCCACTCCTCAAGT[A/G]TTCTAGCTCATGGGG | 140456 |
rs745324502 | in-del | -/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15292244 | ATCCACTGGAAAAAA[-/T]TGGCAAGTGACATGT | 140456 |
rs745344247 | snp | C/T | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316849 | AAGCATCAGACTACT[C/T]GCCATGGTAGTTCCA | 140456 |
rs745345169 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284220 | TCGGGCCACTGCACT[A/C]CAGCCTGGGCGACAG | 140456 |
rs745355699 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15297413 | CACACAGGGGGGTAA[A/G]TTGAAGAGAGAGGAG | 140456 |
rs745357956 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15292972 | TCCGAAGTTATAAGT[A/G]GGGCTCTTTTGTGCC | 140456 |
rs745370216 | snp | C/T | 4.57708e-05 | 0.00478365 | synonymous-codon | ASB11 | GRCh38.p7 | X:15288017 | CTCCACATTGGACTG[C/T]CTCGCTGCAGCATGG | 140456 |
rs745384395 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305494 | TTGGCTAAACATGAA[C/T]GGAGTCTCTGGGTGA | 140456 |
rs745442746 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281791 | CAATCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 140456 |
rs745445940 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284958 | AGCATCCATGAGATA[C/G]AAAGCTACCTGGAGG | 140456 |
rs745471113 | snp | A/G | | | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314931 | AAATGGGTTTAGTGA[A/G]GAGCTTTTCCTGACA | 140456 |
rs745475931 | snp | A/T | 2.30556e-05 | 0.00339518 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315515 | TTAGGAGAGCCAAAA[A/T]AACTTTAATTAAAAG | 140456 |
rs745580483 | in-del | -/A | 2.50416e-05 | 0.00353839 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315641 | GGGTCCTAGGACTGT[-/A]AAATTTCACTGAGTT | 140456 |
rs745625723 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15288232 | CCTCAGCAATGCCTA[C/T]TAAGACTACTTGAAA | 140456 |
rs745727044 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283295 | AGAGCTAAAAGCTAA[A/G]TGGTTTCTACTTGCC | 140456 |
rs745741334 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306173 | TACCCAGTCTGTCAT[C/T]GATGGGCATTTGGGT | 140456 |
rs745742105 | snp | A/G | 2.30646e-05 | 0.00339585 | synonymous-codon | ASB11 | GRCh38.p7 | X:15293267 | ACATGCAGCACTGCC[A/G]CTGCAGCAAGCATTG | 140456 |
rs745766283 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15297149 | ATACAAAAATTAGCC[A/G]GGCGTGGCGGCGTGT | 140456 |
rs745924749 | snp | C/T | 0.000113946 | 0.00754718 | missense | ASB11 | GRCh38.p7 | X:15283596 | AGACACTTCCGGACA[C/T]ACAGGCGGCAGAGCT | 140456 |
rs746004496 | snp | A/G | 0.0026455 | 0.0362733 | | | GRCh38.p7 | X:15276452 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 140456 |
rs746019983 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15283772 | TATAGAATGAGGTAG[C/T]GGACACTAAATACAG | 140456 |
rs746043626 | snp | C/T | 4.78177e-05 | 0.00488943 | intron-variant | ASB11 | GRCh38.p7 | X:15302859 | GACTTCTTCCTGTAA[C/T]TTGTCCATGCTGCCC | 140456 |
rs746118225 | snp | C/G | 2.27884e-05 | 0.00337545 | missense | ASB11 | GRCh38.p7 | X:15283537 | ATCGTTCGAGTGGCT[C/G]TGGCAGATGTAGCTT | 140456 |
rs746154724 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15311339 | CTAAAGGAGACTGGT[A/G]GAAGGTAGAGCCTCT | 140456 |
rs746198119 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15288981 | GATACTGTAGCAGGA[A/T]AGATATAAACTAGCC | 140456 |
rs746210671 | in-del | -/TTC | | | intron-variant | ASB11 | GRCh38.p7 | X:15300095 | AAAGTCTTTTCATTT[-/TTC]TTTTCCTTTTGAGAA | 140456 |
rs746212675 | snp | A/T | 4.64895e-05 | 0.00482106 | intron-variant | ASB11 | GRCh38.p7 | X:15302719 | GGATCAAGTCTTCAG[A/T]TCACTTACTTGTGCA | 140456 |
rs746217575 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316695 | GGCCAGGCTGGTCTC[C/G]AACCCCTGACCTCAG | 140456 |
rs746234152 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15307103 | TTGCAATTAAAAGAG[C/T]TAACATAGGTTATCA | 140456 |
rs746243837 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15307891 | CTTTCATGAAGAGTT[G/T]CTAAAGTAACACAGA | 140456 |
rs746318515 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15287494 | ACCACATCTGGCTAA[G/T]TTCTGTATTTTTAGT | 140456 |
rs746319146 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15285665 | ATCATAATTCTTCTG[A/G]TGAAGATTCAAATAA | 140456 |
rs746322639 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15304549 | TTGATCCCAGGTCTG[A/G]GCCAGGTAAAATACA | 140456 |
rs746330849 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15295281 | CTCTTGATCTCATGA[A/T]CTACCTGCCTCAGCC | 140456 |
rs746415451 | snp | C/G | 0.00211696 | 0.0324653 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316124 | AAAGACCATTTACCT[C/G]GCCGGGCGCGGTGGT | 140456 |
rs746495925 | snp | A/G | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283480 | ATCTGTGTCATTCCA[A/G]GTATCTTCCCAGGAA | 140456 |
rs746557501 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15313644 | AACAAGTAAAGATAT[G/T]TGCACTACAGAATGA | 140456 |
rs746582687 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15281932 | CGAACTCCTGACAGT[A/G]CGATCTGCCTGCCTC | 140456 |
rs746597040 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15300359 | GAATCTTGGTTTAAT[A/G]TTTTACTCACATTTA | 140456 |
rs746607632 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15299402 | AGATTGAAAATTTTT[A/C]TGATTGGCAATTGGT | 140456 |
rs746617167 | snp | G/T | 4.61111e-05 | 0.0048014 | synonymous-codon | ASB11 | GRCh38.p7 | X:15288035 | CGCTGCAGCATGGAG[G/T]GGGGTGTCCAGCCAC | 140456 |
rs746743451 | snp | C/T | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316331 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 140456 |
rs746792409 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15309073 | AGACACACATCACCA[C/T]TCCCAGCTAATTTTA | 140456 |
rs746816460 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15297022 | TACAAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 140456 |
rs746885152 | in-del | -/TA | 3.29511e-05 | 0.00405887 | upstream-variant-2KB, frameshift-variant | ASB11 | GRCh38.p7 | X:15315533 | CTTTAATTAAAAGCT[-/TA]AAGAAAAAAAACGTA | 140456 |
rs746910757 | snp | G/T | 2.47782e-05 | 0.00351973 | intron-variant | ASB11 | GRCh38.p7 | X:15297709 | AAGAAGAGAGTTTAT[G/T]TATTTTTTACAGACT | 140456 |
rs746995962 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15304702 | GGCCAGCATGGTGAA[A/G]CCCTGTCTCTGATAA | 140456 |
rs747034445 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15304811 | ACCCGGGAGGCAGAG[A/G]TTGCAGTGAGCTAAG | 140456 |
rs747061607 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15288932 | GACTCTTGGTTTCTG[C/T]ATATGCCTTTTAGAA | 140456 |
rs747065194 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15301654 | TGGCTTACCTCCTCT[A/G]TATAAATGTAGACCC | 140456 |
rs747124555 | snp | G/T | 0.000252331 | 0.0112295 | intron-variant | ASB11 | GRCh38.p7 | X:15283650 | AGAGAAATAAAAATG[G/T]TGTTAACTTCATAGT | 140456 |
rs747136697 | snp | A/C | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281215 | AAAGAAAAGAAAAGA[A/C]AAAAGTTCATGTATT | 140456 |
rs747332776 | snp | C/G | 2.27881e-05 | 0.00337543 | missense | ASB11 | GRCh38.p7 | X:15283564 | GCTTGTGGATGGCTT[C/G]ATGACATGCTCGACC | 140456 |
rs747340634 | in-del | -/CT | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15315171 | AAGTTTCTCAAAATA[-/CT]CTTAGTAAGCCACTA | 140456 |
rs747360176 | snp | A/G | | | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15315155 | TTGGCTAGTAGAAAT[A/G]AAGTTTCTCAAAATA | 140456 |
rs747363389 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316024 | TGTTCTAAGTGGGAA[A/C]TACTACTCCCTGGAG | 140456 |
rs747372309 | snp | C/T | 2.30736e-05 | 0.00339651 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15314474 | TCTCATTTTCCCCAG[C/T]TAATTGAAGCATTCT | 140456 |
rs747378681 | snp | C/T | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317140 | ACTCTAGGTCTCTGC[C/T]TTCATTCTTGGCTAT | 140456 |
rs747432610 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306519 | GAAACCAGCCTGGCC[A/G]ACATGAAACCCCATC | 140456 |
rs747467201 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15276057 | GTGTCAGCTATTCTC[C/T]TTGCGTTCAATTCAT | 140456 |
rs747503726 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15302673 | GCCAAAGCTAATAAA[C/G]AATGATGTGTAATTA | 140456 |
rs747568562 | snp | G/T | 0.023121 | 0.105004 | intron-variant | ASB11 | GRCh38.p7 | X:15314347 | TTTTTTTTTTTTTTT[G/T]TAACTAGTCAAAGTA | 140456 |
rs747653266 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299277 | CAGCCTAGTTTTATA[C/G]ATTTTAGGGAAACAT | 140456 |
rs747685831 | in-del | -/AC/ACAC | 0.457222 | 0.141144 | intron-variant | ASB11 | GRCh38.p7 | X:15313476 | TTCGTGTATATGTAT[-/AC/ACAC]ACACACACACACACA | 140456 |
rs747737607 | snp | C/T | 0.00422943 | 0.0457911 | | | GRCh38.p7 | X:15280253 | TACTCTCTGTTTCTG[C/T]GAGCTCAATTTTTTT | 140456 |
rs747779199 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15302523 | CAGAGGAAAAGGAGG[C/G]AACTGGGCTGAAAAT | 140456 |
rs747825494 | in-del | -/AAAAG | 0.000529661 | 0.016265 | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281199 | AAAACTTCGTCTCAA[-/AAAAG]AAAAGAAAAGAAAAA | 140456 |
rs747874298 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | ASB11 | GRCh38.p7 | X:15284120 | AGCCGGGTGTGGTGG[C/T]GGGTGCCTATAGTCC | 140456 |
rs747931935 | snp | G/T | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:15276569 | TGATCCGCCCGCCGT[G/T]GCCTCCCAAAGTGCT | 140456 |
rs747944502 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15303865 | GTAGAGCAGTGCCAT[A/G]AGGAACAGCCTTAGA | 140456 |
rs747964838 | in-del | -/TT | | | intron-variant | ASB11 | GRCh38.p7 | X:15302383 | CAATAGCTGACTAAC[-/TT]AGCTTCAGGACTGCT | 140456 |
rs747975637 | snp | A/G | 2.2811e-05 | 0.00337713 | missense | ASB11 | GRCh38.p7 | X:15289579 | GAGTTCCGAGCTGAG[A/G]CACCTCATGGTCAAT | 140456 |
rs748031033 | snp | A/G | | | | | GRCh38.p7 | X:15278727 | AGGAAGAGACTGTCC[A/G]TTCTTTCCTCTTTGA | 140456 |
rs748037795 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15290451 | AGTCTGAAAAATACC[A/T]ATGAGAAAGAATAAA | 140456 |
rs748082037 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15284056 | AGGAGATGGAGACCA[C/T]CCTGGCTAACACGGT | 140456 |
rs748146358 | snp | C/G/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15296948 | CACTGTTCACAATTG[C/G/T]AAAGACCTGAAAGCA | 140456 |
rs748208221 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15307368 | GTTTCATGGAAGACA[A/G]TTTTTCCACAGATGA | 140456 |
rs748333039 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15306340 | CAGATAAAAATTTTT[A/G]ACATGAGCATATATT | 140456 |
rs748490330 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15292069 | GAAAGACATTTATAT[A/C]ATTTCCAAAGTAGTT | 140456 |
rs748526679 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15301182 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 140456 |
rs748543834 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15301580 | CAGTGCACCCAGTGG[A/T]TTAAATTCAAAGTAG | 140456 |
rs748544728 | in-del | -/TTT | 0.0115102 | 0.074984 | intron-variant | ASB11 | GRCh38.p7 | X:15314330 | TATCAGAAGCATTAC[-/TTT]TTTTTTTTTTTTTTG | 140456 |
rs748577195 | in-del | -/A | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15275979 | AGAGCATCCTCCCCC[-/A]ACAAGTTGTGGTTAT | 140456 |
rs748613252 | snp | C/T | 9.32999e-05 | 0.00682944 | utr-variant-5-prime, intron-variant | ASB11 | GRCh38.p7 | X:15314497 | AGCATTCTGATGCTT[C/T]GTCCTTGGAGGTCTT | 140456 |
rs748666933 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15275478 | TGTGCATTTATATAT[A/G]TATATATGTGTATAC | 140456 |
rs748788870 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15285451 | GCCAGTATTAATCTT[C/T]CTAGAGCAAGTGGCT | 140456 |
rs748791818 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306386 | CTTGTCTTTAGTTGG[C/T]TGAAAGCTGACAAGT | 140456 |
rs748809669 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15312634 | AATAGCATATGCTAG[A/C]AGACTCAAGAAACTT | 140456 |
rs748818837 | snp | A/G | | | utr-variant-5-prime, intron-variant | ASB11 | GRCh38.p7 | X:15314523 | GTCTTATTTCTTTAG[A/G]TAAGACTGCTGTTGT | 140456 |
rs748842406 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15297956 | AGAAGTAGAAGTTAC[A/G]ATCAGGGGAGCCTAA | 140456 |
rs748865440 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15296048 | GGAGTCTGAAACCAG[C/T]ATCGCTGGTTTCACT | 140456 |
rs748905741 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15288915 | TATTTCATTTTTCCA[C/T]GGACTCTTGGTTTCT | 140456 |
rs749037811 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15302964 | GTCAGCCACTTTCAG[A/G]GAGACAAGCTACTGA | 140456 |
rs749132047 | snp | G/T | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15283164 | CCACCTGAATTTATA[G/T]GTGTCTATACAATAT | 140456 |
rs749157582 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15284049 | CGAGGTCAGGAGATG[A/G]AGACCATCCTGGCTA | 140456 |
rs749183058 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299080 | ATAACCTGATTTTAA[A/C]AACTTGGCTCTTACC | 140456 |
rs749206732 | in-del | -/CTAAA | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15289140 | GGCTGAAATCTAGGC[-/CTAAA]CTAATCAATATATTG | 140456 |
rs749247892 | in-del | -/AG | | | intron-variant | ASB11 | GRCh38.p7 | X:15297403 | TGAATATTTACACAC[-/AG]GGGGGTAAGTTGAAG | 140456 |
rs749258737 | snp | A/G | | | downstream-variant-500B | ASB11 | GRCh38.p7 | X:15281408 | CATACCATTGCACTC[A/G]AGCCTGGATGACAAA | 140456 |
rs749275803 | snp | A/G | 2.42878e-05 | 0.00348472 | intron-variant | ASB11 | GRCh38.p7 | X:15293149 | ATCAATGTTTCACAT[A/G]CATTGTGGTGGCTCA | 140456 |
rs749334609 | in-del | -/AGAA | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15295427 | ACTTGGGAAAAACTT[-/AGAA]AGTAAAATTAGCAGG | 140456 |
rs749361449 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316771 | TGAGCCACTGCACCC[A/G]GCCAAGCCTGTATTT | 140456 |
rs749377377 | in-del | -/A | 0.000205822 | 0.0101424 | frameshift-variant, intron-variant | ASB11 | GRCh38.p7 | X:15314435 | TCCGGACCTTCTGAT[-/A]ACGTTCTGAAACTTC | 140456 |
rs749423835 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15286421 | CCTGTAATCCCAGCA[C/T]TTTGGAAGGCTGAGG | 140456 |
rs749463560 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284109 | TACAAAAAATTAGCC[C/G]GGTGTGGTGGCGGGT | 140456 |
rs749467059 | snp | A/G/T | 0.000145905 | 0.00854011 | missense | ASB11 | GRCh38.p7 | X:15297596 | CCATTTTCCAATAAG[A/G/T]CTTTGGCACAGGCCA | 140456 |
rs749468210 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15292114 | TTAAAGGACTTACAT[A/G]ATGTTTGGGAAATGA | 140456 |
rs749504529 | snp | C/G | | | | | GRCh38.p7 | X:15275357 | AATCCTGATTCTAGC[C/G]CTGGTGAAGGATCAT | 140456 |
rs749531589 | snp | C/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15276565 | CTCGTGATCCGCCCG[C/T]CGTGGCCTCCCAAAG | 140456 |
rs749548690 | snp | C/T | 2.3546e-05 | 0.0034311 | intron-variant | ASB11 | GRCh38.p7 | X:15302708 | ATAAGCATGAAGGAT[C/T]AAGTCTTCAGTTCAC | 140456 |
rs749556194 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15293491 | TATTGGGTGGATCGA[A/G]CGAGTTACTATATGT | 140456 |
rs749661734 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15300410 | TACTCATATCGGTTT[A/G]ATGTTTTACTCACAT | 140456 |
rs749663689 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15308855 | CCTGGGCCATTCCGT[A/G]GCCTGTTAGGAACCG | 140456 |
rs749726261 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15287229 | TTGCCATCAGATTGT[C/T]TCCCAATATTACAAA | 140456 |
rs749744149 | snp | C/T | 2.4455e-05 | 0.0034967 | intron-variant | ASB11 | GRCh38.p7 | X:15287872 | AATGGATACCCAGCC[C/T]TTGGTTACCTTCACG | 140456 |
rs749788594 | snp | A/G | 2.28167e-05 | 0.00337755 | missense | ASB11 | GRCh38.p7 | X:15287995 | AGTCGGTTAGCAGGT[A/G]GATGACCTCCACATT | 140456 |
rs749819981 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282092 | AGTAGCAATTCTCCC[C/T]CAGTTGTTGCAACTA | 140456 |
rs749856483 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15307967 | TGGCCTTTTCCCACT[C/G]CCAGGGCAGGGTATG | 140456 |
rs749929531 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15302587 | AGGAGAGGCAGTGAG[A/G]TATGAGAGGACATAC | 140456 |
rs749942633 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314786 | TCTCACCACAATTAA[A/G]GTAAATCATTTCTTG | 140456 |
rs749965793 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15294016 | GTACTCTAAAACTTA[A/C]AGTATAATAAAAAAT | 140456 |
rs750006166 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15290656 | CTTGCAAAGAGTTAG[C/T]TCTCTTTGAAGATTT | 140456 |
rs750022499 | snp | C/T | 4.55789e-05 | 0.00477361 | synonymous-codon | ASB11 | GRCh38.p7 | X:15283514 | TTAGGACTATTGGTA[C/T]AGGAGGAATCGTTCG | 140456 |
rs750028021 | snp | C/T | 2.28527e-05 | 0.00338021 | missense | ASB11 | GRCh38.p7 | X:15302778 | CCTGAGCTGCAGCTT[C/T]ATGAAGTGGGGATCG | 140456 |
rs750056130 | in-del | -/G | 0.00896606 | 0.0663524 | intron-variant | ASB11 | GRCh38.p7 | X:15301540 | AGACAGAGAGAGAGA[-/G]AGAAAGAAAAAGAGA | 140456 |
rs750056285 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15310748 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCAGGTG | 140456 |
rs750199601 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306736 | CAACAACAACAACAA[C/T]TCTTTGGATATTTAT | 140456 |
rs750242896 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15307385 | TTTTCCACAGATGAG[A/G]GTGGGCAGGGGATGG | 140456 |
rs750262142 | in-del | -/GAC | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15280584 | TGCTGAATCATACTT[-/GAC]GACAACAACAAAACA | 140456 |
rs750289619 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15298720 | TAACAGTAGGTATGA[A/G]GTATAGATGATGGAG | 140456 |
rs750319989 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15294954 | GGAAACAATGATAAG[A/G]CAATTGCCTCTCCTT | 140456 |
rs750355310 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15301877 | TTGTTCTTAAAATAG[C/T]GTATCATTGGGATAG | 140456 |
rs750399842 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15285875 | CTGGGCGTGGTGGCA[C/T]GCGCCTGTAATCGCA | 140456 |
rs750404236 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15284994 | ACAATCGATCTTAGT[G/T]AAAATCTTGGGAAGC | 140456 |
rs750467657 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15312613 | TTGCTGACAATAGTT[C/T]ACAGGAATAGCATAT | 140456 |
rs750516433 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15298028 | TTAATTCTGCATTCT[A/G]GAGCAGGTAATGTAC | 140456 |
rs750567046 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284086 | TGAAACCCCGTGTCC[A/G]CTAAAAATACAAAAA | 140456 |
rs750575414 | snp | A/G | | | | | GRCh38.p7 | X:15280755 | TATCATCTTACCCCA[A/G]TTAGAATGGCTATCC | 140456 |
rs750601966 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15289693 | TATTAAATATTAACA[A/G]AATTATAGGATTGCT | 140456 |
rs750642402 | snp | A/T | 2.29487e-05 | 0.0033873 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15314458 | GAAACTTCACAATTC[A/T]TCTCATTTTCCCCAG | 140456 |
rs750693644 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15290238 | AGCACAGTTGAAATC[A/G]CTCTCCAGAATGATG | 140456 |
rs750751415 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15305911 | GTTATTTTTCCTGAT[C/T]GTCTCACTCCTCCTA | 140456 |
rs750759835 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15296052 | TCTGAAACCAGCATC[A/G]CTGGTTTCACTAAAA | 140456 |
rs750843640 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15289800 | AGGCTGAGACCGGCG[A/G]ATTCCCTGAGGTCAG | 140456 |
rs750886526 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15304427 | GATTTTCAATATATC[C/T]AGATATAAAAGTAAA | 140456 |
rs750895396 | snp | A/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15276891 | CTTCAAACATTTTTG[A/G]AGATTTATTTTAAAA | 140456 |
rs750959070 | snp | A/C | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282397 | GAGAAGAAGGAGAAG[A/C]CAGAAAAGGAGAAGC | 140456 |
rs751046923 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15301075 | TCAAACGATTTTCCT[C/G]CCTCAGCCTCCCAAG | 140456 |
rs751118483 | in-del | -/A | | | intron-variant | ASB11 | GRCh38.p7 | X:15292034 | CACGAGACTCTGTCG[-/A]AAAAAAAAAAAAAAA | 140456 |
rs751161514 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15287571 | ACCTTGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 140456 |
rs751172542 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15302191 | GAGTGAGTTTGAAAG[C/T]AGATCCTGCCCGCCT | 140456 |
rs751230402 | snp | A/C | | | | | GRCh38.p7 | X:15277476 | ATTAATTGAGAAGCT[A/C]TCTTAGGGCACTTCA | 140456 |
rs751253375 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282968 | CATGTGTGTGTGTGT[A/G]TATATATACGTATAT | 140456 |
rs751292804 | snp | C/T | 6.83698e-05 | 0.00584639 | missense | ASB11 | GRCh38.p7 | X:15283512 | ACTTAGGACTATTGG[C/T]ATAGGAGGAATCGTT | 140456 |
rs751329422 | snp | C/T | 0.00013946 | 0.00834929 | upstream-variant-2KB, synonymous-codon | ASB11 | GRCh38.p7 | X:15315546 | CTTAAAGAAAAAAAA[C/T]GTAGCAAACATTGTA | 140456 |
rs751351304 | snp | C/T | 0.000114396 | 0.00756206 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15314437 | CCGGACCTTCTGATA[C/T]GTTCTGAAACTTCAC | 140456 |
rs751361645 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ASB11 | GRCh38.p7 | X:15314749 | AGTGACAGGGATATC[C/T]GACTCATTTACTTTT | 140456 |
rs751374438 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15311331 | GAGCTGAGCTAAAGG[A/T]GACTGGTGGAAGGTA | 140456 |
rs751386464 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | ASB11 | GRCh38.p7 | X:15292919 | GGCCTGCCAATAGAC[C/T]ATCCCCAGGAAATGG | 140456 |
rs751388058 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15306037 | GCATTTGGTTTTCTG[A/T]TCCTGTTAGTTTTCT | 140456 |
rs751391973 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15285285 | AGGTGGGATTACAGG[C/T]GGGTGCCACCAAACC | 140456 |
rs751433388 | snp | A/G | 4.55773e-05 | 0.00477353 | synonymous-codon | ASB11 | GRCh38.p7 | X:15283580 | ATGACATGCTCGACC[A/G]AGACACTTCCGGACA | 140456 |
rs751473325 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15304178 | ATAAACTTGGTGAAA[C/T]GAAAATCCCAGCAAA | 140456 |
rs751486927 | snp | A/C | 2.28702e-05 | 0.00338151 | missense | ASB11 | GRCh38.p7 | X:15302790 | CTTCATGAAGTGGGG[A/C]TCGATCAGCCCAGCA | 140456 |
rs751518557 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284872 | ACTGTAACAGCATCT[C/T]ACACCCCATGAAAAA | 140456 |
rs751537508 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15293877 | AACATCACACACCGG[A/G]GACTGTTGTGGGGTG | 140456 |
rs751634757 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15284473 | CAAAGTACTCCTGGA[C/G]CTACCGGCTCTAGCT | 140456 |
rs751715288 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15298490 | GCCTTGATTTCCAAA[A/C]AAGGAGGGCATGTCT | 140456 |
rs751832282 | snp | C/T | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282478 | AATATTGACCCAGCA[C/T]TGAGCCCACTTTGGT | 140456 |
rs751843011 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15303382 | TCTCGTAAGTTTTAC[A/G]AAAATTTATGAATTT | 140456 |
rs751880598 | in-del | -/TAGG | | | intron-variant | ASB11 | GRCh38.p7 | X:15305601 | AAAAAAAAGATTAGA[-/TAGG]TAGATAGATAGATAG | 140456 |
rs751929225 | snp | C/T | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15276549 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCGCCCG | 140456 |
rs751935931 | in-del | -/CAAA | | | intron-variant | ASB11 | GRCh38.p7 | X:15284976 | AGCTACCTGGAGGAC[-/CAAA]CAATCGATCTTAGTT | 140456 |
rs752006100 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15293106 | GACTAACACTAGACC[A/T]TTGATTCATACAGAT | 140456 |
rs752010906 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | ASB11 | GRCh38.p7 | X:15312488 | ATTTAATGAGGCATG[G/T]GGTGTTAAATGCAGC | 140456 |
rs752044536 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15284024 | TTGGGAGGCCAAGGT[A/G]GGCGGATCACGAGGT | 140456 |
rs752079475 | snp | C/T | 2.36398e-05 | 0.00343793 | missense | ASB11 | GRCh38.p7 | X:15293316 | TGAACTGTCACTCCA[C/T]TGACCTAATGATGGG | 140456 |
rs752089982 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15291228 | ATATACAGAGACACA[C/G]AAATTATGTGTTTAT | 140456 |
rs752140366 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15308613 | CTTGCTTTGCTGAAT[C/G]GTAACACCCCAAAAT | 140456 |
rs752141937 | snp | G/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15317420 | TTGAGTCGTCTTAAC[G/T]CTCAAGGAACAGACA | 140456 |
rs752188890 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15287557 | GTCTCAAACTCCTGA[A/C]CTTGTGATCCACCCG | 140456 |
rs752301930 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15305400 | TGAGGAACAGTTCCA[C/G]ATTGAAAGGGATGAC | 140456 |
rs752422276 | snp | C/T | 2.30678e-05 | 0.00339608 | missense | ASB11 | GRCh38.p7 | X:15293221 | GCACCTCCAACTGGG[C/T]CTTGGCTCCGAACTC | 140456 |
rs752455840 | snp | C/G | 2.30128e-05 | 0.00339203 | intron-variant | ASB11 | GRCh38.p7 | X:15283657 | TAAAAATGGTGTTAA[C/G]TTCATAGTGGTGGGA | 140456 |
rs752468109 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15291697 | GTGAGACAGAGCAAG[A/G]CTCTGTCTCAAAAAA | 140456 |
rs752470054 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15301382 | AAGTGATAAAATCAG[A/G]TACAAAGTTCATTTG | 140456 |
rs752542312 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | ASB11 | GRCh38.p7 | X:15314072 | CAAAAAAAAAAAAAA[A/C]AAAAAAGAGTGCACT | 140456 |
rs752557808 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | ASB11 | GRCh38.p7 | X:15292586 | AGTCAGCTTCAAGAT[C/T]ACCAATGCTATACTT | 140456 |
rs752566105 | snp | A/T | 2.29108e-05 | 0.00338451 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15314448 | GATACGTTCTGAAAC[A/T]TCACAATTCTTCTCA | 140456 |
rs752652002 | snp | C/T | 2.27892e-05 | 0.00337551 | missense | ASB11 | GRCh38.p7 | X:15283590 | CGACCGAGACACTTC[C/T]GGACACACAGGCGGC | 140456 |
rs752677085 | snp | C/T | | | missense | ASB11 | GRCh38.p7 | X:15289622 | TGCCAGCAGGATCTC[C/T]ATGCACTCTCTGTGA | 140456 |
rs752795626 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305952 | TCCAATAGGCCCCAG[C/T]GTATGTTGTTCCCCT | 140456 |
rs752867474 | snp | C/G | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15278201 | CGTATCACAGTGATT[C/G]GTTTACTGCATGCAA | 140456 |
rs752880508 | snp | C/T | 0.00370173 | 0.0428621 | | | GRCh38.p7 | X:15279239 | AGGTTCTTTCCTTAA[C/T]ATCTTCTAAAAAATG | 140456 |
rs752883631 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15308890 | GCACAGCAGGAAGTG[A/G]GCAGCAGGTGAGCAA | 140456 |
rs752884454 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15297406 | ATATTTACACACAGG[C/G]GGGTAAGTTGAAGAG | 140456 |
rs752897584 | snp | G/T | 4.56324e-05 | 0.00477641 | missense | ASB11 | GRCh38.p7 | X:15287968 | CATTTCTACGCTTCA[G/T]GTTAGCTCCATAGTC | 140456 |
rs752913561 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15284816 | TCTTCAAGAAAACCT[A/G]ATTACTGGTCTACAC | 140456 |
rs752998436 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15310856 | AGCCAGTGTGGTGGC[A/G]GGCGCCTGTACTCCC | 140456 |
rs753082019 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15298383 | GGCAGGGCCACAGTC[A/G]GATTTCTGGAACAGA | 140456 |
rs753117272 | snp | A/C | 0.016289 | 0.0887646 | intron-variant | ASB11 | GRCh38.p7 | X:15312462 | AAAGGTTTTACAGCA[A/C]AAAGAATGATATTTA | 140456 |
rs753146104 | snp | C/T | | | | | GRCh38.p7 | X:15277652 | CGCCCTGCTTGCTTT[C/T]GGTGGCTTGCTTTTT | 140456 |
rs753191960 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15310870 | CGGGCGCCTGTACTC[C/T]CAGCTACTCAGCAGG | 140456 |
rs753272970 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15295303 | GCCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 140456 |
rs753292629 | snp | A/G | 0.00581083 | 0.0535878 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316544 | CAATGGTGCGATCGC[A/G]GCTCACTGCAACCTC | 140456 |
rs753368327 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15305747 | ATTATATGCAATAGA[C/T]ATCATCAATTTTATG | 140456 |
rs753381423 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15295098 | GCCAGGCTGGAGTGC[A/G]GTGGTGTGATCTCGG | 140456 |
rs753385116 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15315927 | TATGTTAGAAAGCAG[C/G]GTTGGAAAGATAGAA | 140456 |
rs753456497 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15289746 | TAACCTAGGTTGGCC[A/G]GGTGTGGTGGCTCAC | 140456 |
rs753473692 | snp | C/T | 7.41977e-05 | 0.00609043 | intron-variant | ASB11 | GRCh38.p7 | X:15297536 | ATTAACAGATGCATC[C/T]GGCCAGACAGACCCA | 140456 |
rs753502208 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15294248 | CCTCTGATGCCATTG[A/C]AATATAGGACAGTCA | 140456 |
rs753567517 | snp | C/T | 2.32412e-05 | 0.00340882 | missense, intron-variant | ASB11 | GRCh38.p7 | X:15297650 | TGGAGAGAAGACACC[C/T]GGTTAATTGTCACAA | 140456 |
rs753601440 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299976 | TTCATCATAAGGCCT[-/C]TTTTTGACTCCTGAA | 140456 |
rs753684357 | snp | G/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15300280 | GAAAATGGAGGAGTA[G/T]AATGTTCAAATACTT | 140456 |
rs753708746 | snp | A/G | 2.31957e-05 | 0.00340548 | intron-variant | ASB11 | GRCh38.p7 | X:15283669 | TAACTTCATAGTGGT[A/G]GGAGGTGGGGTGGAA | 140456 |
rs753727055 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15307523 | TATGAGAATCTAATG[C/G]CACCACTGATCTGAC | 140456 |
rs753753313 | snp | C/T | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316671 | GTAGAGACGAGGTTT[C/T]GCCATGTTGGCCAGG | 140456 |
rs753808708 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15298653 | AGGAGAGCCACAGAG[A/G]TGTCACTATGAGTCT | 140456 |
rs753830418 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | ASB11 | GRCh38.p7 | X:15304498 | TTTTAGCATGGTGCA[C/T]TGAGAAAACCTGAAC | 140456 |
rs753918444 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15313748 | TAAGGAGGTTTTATA[A/C]CTTTTTTAAGAGTGC | 140456 |
rs753953354 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15309005 | TACTGCAACCTCTGC[C/T]TCCCAGGTTCAAGAG | 140456 |
rs753967010 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15305121 | AAAAGGAACAGGGAT[-/A]ATTTTATAGAACAGA | 140456 |
rs753992167 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284659 | AGAATCATCATGCCC[A/G]TGGCTTTGAATGGCT | 140456 |
rs754031878 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15284203 | CTTGCAGTGAGCCGA[C/G]ATCGGGCCACTGCAC | 140456 |
rs754206789 | snp | A/G | 2.31984e-05 | 0.00340568 | missense | ASB11 | GRCh38.p7 | X:15289512 | AAATTACCTAATTCT[A/G]GAAGTTTCTTCACAC | 140456 |
rs754227640 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282977 | GTGTGTATATATATA[C/T]GTATATATATATACG | 140456 |
rs754271833 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | ASB11 | GRCh38.p7 | X:15288758 | GGTGTAGTGGTGTGC[A/G]TCTGTAATCCCAGCT | 140456 |
rs754326644 | snp | A/C | | | intron-variant | ASB11 | GRCh38.p7 | X:15296332 | AAATTAGTTTTCACA[A/C]GGAAGACTTTTATAT | 140456 |
rs754331805 | in-del | -/CAGAAAACTAAAAA | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15296817 | AGTTTGGAGGTTCAT[-/CAGAAAACTAAAAA]CAGAGATACCATATG | 140456 |
rs754373413 | snp | A/G | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:15278107 | TAAGGCTTATCTTTG[A/G]GAAGGTGGATTTGAG | 140456 |
rs754468682 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316545 | AATGGTGCGATCGCG[A/G]CTCACTGCAACCTCT | 140456 |
rs754522790 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | ASB11 | GRCh38.p7 | X:15286000 | ACAAGAGCAAAACTC[C/T]GTCTAAAATAATAAT | 140456 |
rs754528949 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15302271 | AGACCCAGAGCCAGA[A/G]TCACCTAGCTAAGCT | 140456 |
rs754547161 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15287231 | GCCATCAGATTGTCT[C/T]CCAATATTACAAAGC | 140456 |
rs754559674 | in-del | -/CTACTC | | | upstream-variant-2KB | ASB11 | GRCh38.p7 | X:15316844 | ACTAGAAGCATCAGA[-/CTACTC]GCCATGGTAGTTCCA | 140456 |
rs754675422 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | ASB11 | GRCh38.p7 | X:15290384 | ATCTCTCATTCTCTT[C/T]TTTATCCATGCATGT | 140456 |
rs754699654 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15311500 | TGGGCAAGAATGAAA[C/T]TAAGGCGATCCTATT | 140456 |
rs754711645 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15300689 | GTTTAGTCAGTGGTA[-/T]TGTATCAATGTTAAC | 140456 |
rs754721096 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15285498 | AGGACAGAGGAGCTA[A/G]GCCCTGTCCAGGATA | 140456 |
rs754721150 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15295120 | TGATCTCGGCTCACT[A/G]CAACCTCCGCCTCCT | 140456 |
rs754727042 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15301023 | CTGGAGTGAAGTGAC[A/G]CGATCTCGGTTCACT | 140456 |
rs754732499 | snp | C/G/T | 4.55776e-05 | 0.00477358 | synonymous-codon, missense | ASB11 | GRCh38.p7 | X:15283586 | TGCTCGACCGAGACA[C/G/T]TTCCGGACACACAGG | 140456 |
rs754787589 | snp | C/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15314263 | AAGCCCTTGCCCAAA[C/T]TGACAAATTAAATTA | 140456 |
rs754823761 | snp | A/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15295623 | TGCACTGAGTTTGAG[A/G]TATTCATGGGACTGC | 140456 |
rs754833798 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15291516 | TCTGAGACCAGCCTG[A/G]CCAACATGATGAAAC | 140456 |
rs754875163 | snp | A/G | 2.28802e-05 | 0.00338224 | stop-gained | ASB11 | GRCh38.p7 | X:15302793 | CATGAAGTGGGGATC[A/G]ATCAGCCCAGCAATC | 140456 |
rs754889438 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15307577 | TGTCCCTCACCTGCC[A/G]CTCACCTCCTGCTGT | 140456 |
rs754889462 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15299161 | ACAGTCAAACTATAA[A/G]ATATTTGAAGAGATT | 140456 |
rs754928548 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15288391 | AAAAGATAAAGCTAA[C/G]TTTATTTAGTATTTA | 140456 |
rs754944368 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15306204 | TGAGTCCATGTCTTT[C/G]TTATTGTGATTAGTG | 140456 |
rs754956809 | in-del | -/TT | 2.35266e-05 | 0.00342969 | upstream-variant-2KB, frameshift-variant | ASB11 | GRCh38.p7 | X:15315468 | TATCCTAGCCGCTTC[-/TT]TTCTATTTCCTTTGA | 140456 |
rs754998397 | snp | A/G | 4.55789e-05 | 0.00477361 | missense | ASB11 | GRCh38.p7 | X:15283513 | CTTAGGACTATTGGT[A/G]TAGGAGGAATCGTTC | 140456 |
rs755036363 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15296835 | AAAACTAAAAACAGA[C/G]ATACCATATGATCCA | 140456 |
rs755075762 | in-del | -/TAGT | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:15277196 | ATATACATATGTGAG[-/TAGT]TAGTTATTCCAAAAT | 140456 |
rs755120002 | snp | C/T | | | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282620 | TGGGGACACCCAGTG[C/T]TCTCAATCCTAGAAC | 140456 |
rs755130652 | snp | G/T | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:15278155 | CTTGCTTGGCAGCCT[G/T]GTGAATAAATCTTTT | 140456 |
rs755198846 | snp | G/T | 2.49147e-05 | 0.00352941 | intron-variant | ASB11 | GRCh38.p7 | X:15287843 | AAGGGGAGAGAATGT[G/T]CTTATGGAAGAGGAA | 140456 |
rs755216673 | snp | A/C | 2.43757e-05 | 0.00349102 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315596 | CATAGAAAACAGGAC[A/C]ATCTTCCATTTTGGC | 140456 |
rs755229034 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | ASB11 | GRCh38.p7 | X:15313574 | CAATAATTGAAAAAT[A/G]TTTTTGACCTTAGAA | 140456 |
rs755285639 | snp | C/G | | | intron-variant | ASB11 | GRCh38.p7 | X:15293126 | TTCATACAGATTGGA[C/G]TGAGCCCATCAATGT | 140456 |
rs755302907 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | ASB11 | GRCh38.p7 | X:15309840 | AGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 140456 |
rs755326049 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | ASB11 | GRCh38.p7 | X:15288842 | GTGAGCTGAGGTCAC[A/G]CCATTGCACTCCAAC | 140456 |
rs755326107 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-3-prime | ASB11 | GRCh38.p7 | X:15282978 | TGTGTATATATATAC[A/G]TATATATATATACGT | 140456 |
rs755342478 | snp | A/G | | | | | GRCh38.p7 | X:15276042 | GGTGATGTCTCTGAA[A/G]TGTCAGCTATTCTCT | 140456 |
rs755399000 | snp | G/T | 0.0026455 | 0.0362733 | | | GRCh38.p7 | X:15275421 | AATATATGGATATGT[G/T]TTAATCATATATGAG | 140456 |
rs755412962 | snp | A/G | 2.36022e-05 | 0.00343519 | upstream-variant-2KB, missense | ASB11 | GRCh38.p7 | X:15315463 | TCTGCTATCCTAGCC[A/G]CTTCTTTTCTATTTC | 140456 |
rs755478009 | snp | A/T | | | intron-variant | ASB11 | GRCh38.p7 | X:15308709 | ACCCTAGTTATGGGG[A/T]CTTTAGAACACACCT | 140456 |